Time\:14\:00 GMT
Global food and beverage manufacturers are on high alert. Business challenges facing companies today include increased regulatory reporting requirements\, concerns over food safety and accurate nutritional label content\, as well as poor raw material data traceability\, and cumbersome collaboration across the global supply chain.
Many leading food and beverage manufacturers successfully implement Product Lifecycle Management (PLM) for Process integrated product development tools and automated supplier collaboration capabilities. The case study by Tyson Foods demonstrates the advantages of these solutions.
Rapid growth presented the company with a maze of challenges to overcome. Discover firsthand how Tyson Foods leveraged PLM to achieve the following benefits\:
•Accelerated time to market
•Improved collaboration and reduced cycle times
•Empowered decision-making by improving visibility
•Shortened time needed to complete audits
•Minimised risk by bolstering supply chain contingency planning
•Decreased ingredient and packaging costs
The webinar will be followed with a live Q&\;A session\, this is your chance to get your questions answered. Make the most of it\, register today!
The Speakers\:
Kimberly Glenn\, Director of Research and Development\, Tyson Foods. Kim started her career at Hudson Foods developing products for national account customers and wholesale clubs. With the acquisition of Hudson in 1997\, she came to Tyson Foods to develop items for the school foodservice and hospitality arenas. In 2004\, she took on the challenge of serving as business lead for a product data management implementation program. Since early 2007\, Kim has served as Director of R&\;D responsible for Regulatory Labelling and Specifications\, Nutrition Services\, Sensory Insights group\, and the Product Data Management software suite.
Wes Frierson is the Director of Product Strategy for Oracle's PLM for Process solution. In the past\, Wes worked in Product Development and Consulting roles helping to develop and deploy the product around the world. Wes has extensive experience in the Consumer Goods and Retail industries\, having worked with industry leaders such as Heinz\, Coca-Cola\, Tyson\, and McDonald's.
Peter Verstrate\, Senior Manager\, Kalypso. Peter brings over 20 years experience in the FMCG industry holding senior management positions in product development\, quality management\, production and sourcing. Prior to joining Kalypso\, Peter worked for Campofrio Food Group\, Smithfield Food\, Sara Lee and Ahold. He holds an MSc in food technology from Wageningen University.
Technical Requirements
- PC headset
- PC speakers
- Broadband Connection
Intended audience\: Directors of Supply Chain\, Operations\, Innovation\, Research and Development\, and Quality in the Food &\; Beverage and Retail sectors.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T172159Z DTSTART;VALUE=DATE-TIME:20100928T111900Z DTEND;VALUE=DATE-TIME:20020203 UID:http://www.webinarcentral.net/content/ondemand-webinar-reduce-it-infrastructure-costs-using-application-portfolio-management URL;VALUE=URI:http://www.webinarcentral.net/content/ondemand-webinar-reduce-it-infrastructure-costs-using-application-portfolio-management SUMMARY:OnDemand Webinar\: Reduce IT infrastructure costs using Application Portfolio Management DESCRIPTION:Application retirement is a major paradigm shift toward holistically managing the enterprise application portfolio which allow companies to retire seldom-used applications to significantly cut hardware\, storage and software maintenance costs in addition to indirect expenditures such as power\, space\, etc. Enterprises across a variety of industries are looking for ways to reduce IT expenditures
In this seminar we will talk about new innovations that will simplify and streamline the application retirement process\, allowing for measurable ROI and reduced TCO. This seminar will also show you how to compute the ROI by adopting a process-oriented approach to retire legacy applications.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T172159Z DTSTART;VALUE=DATE-TIME:20100928T180000Z DTEND;VALUE=DATE-TIME:20100928T190000Z UID:http://www.webinarcentral.net/content/how-use-foreign-trial-data-your-nda-approval-process URL;VALUE=URI:http://www.webinarcentral.net/content/how-use-foreign-trial-data-your-nda-approval-process SUMMARY:How to Use Foreign Trial Data in Your NDA Approval Process DESCRIPTION:In this NDA Approval Process training Webinar learn the guidance and regulations governing FDA's acceptance of foreign trial data and know how FDA implementing these rule along with design considerations and requirements for foreign trials.
Why Should You Attend\:
While the law allows 100 percent of pivotal data to come from foreign trials\, there have been very few such submissions accepted by FDA – mainly in limited therapeutic areas. Given lower costs and shorter recruiting times\, the use of foreign sites is appealing to all drug developers\, especially generic and 505(b)(2). Due to shortcomings found during site inspections\, lack of inspection resources and the general tightening of FDA safety reviews\, FDA has started imposing some “unwritten” requirements for the acceptance of such data. This webinar explores these requirements and how you can ensure compliance.
Areas Covered in the Seminar \:
The purpose of the FDA inspection is a verification activity that should demonstrate to the regulatory agency and provide assurance that products consistently meet quality expectations and that your company is operating in a consistent and compliant state of control.
The key to a successful audit is being able to communicate how your quality systems assure this state of control.
However\, the arrival of an investigator for an inspection can still be an intimidating experience. The inspection can be less traumatic if the site and its personnel are properly prepared for the inspection and the investigator. During this hour presentation\, you will find out how to prepare for the inspection and minimize stress\, disorder\, and any misinterpretation by the investigator during the inspection with careful planning of activities and effective resource development will support a successful inspection.
Why you should attend\:
* Recognize the purpose of the inspection
* Learn how to properly communicate with the inspector
* Anticipate what information the investigator can and will request
* Know how to keep the inspection from being an “emotional” event.
* Know what is expected of you and your company
* Learn what not to say or do during an inspection.
* Recognize your audit responsibilities and vulnerabilities
* Identify the internal support system of a successful inspection
* Realize what steps you/your company should take to prepare for a successful inspection
Areas Covered in the Session\:
* Expectations of an audit
* Why the FDA conducts inspections
* Pre-planning and preparation activities
* What to do when the investigator arrives
* What documents to have ready and on hand
* Assignments and responsibilities for the inspection
* A review of Inspection Do's and Don'ts
* The Opening and Close-out Sessions
* Actions to take after the inspection is over
Who Will Benefit\:
* Site Quality Operations Managers
* Quality Assurance personnel
* Plant Managers
* Manufacturing Superintendents and Managers
* Individuals whose job knowledge and/or expertise may be required during an audit (Subject Matter Experts)
One of the most common reasons noted by the FDA for recalls of medical device is improper validation.
It is also one of the most common reasons companies receive 483s and warning letters. Conversely\, successful validations not only satisfy compliance and regulatory requirements\, they also provide for robust manufacturing processes satisfying the needs of many individual functions within your organization How do we get there? After we have a clear understanding of the regulatory intent of validation\, the key for a robust process validation is the use of six sigma techniques and risk management. The rigor of a validation should be tied to the individual risk assessments of your products Critical Quality Attributes laid out in your design controls. Using the GHTF Process Validation Guidance document as a backdrop\, this seminar will provide a review of the fundamentals of validation\, provide guidance on using a risk classification scheme to define the rigor of testing and provide a guidance on the use of Six Sigma tools to create and sustain a state of validated control.
Why you should attend\:
* Did you know that poor or ineffective Process Validation was one of the top citations noted in recent FDA warning letters and 483s?
* Do you know that poor or ineffective Process Validation also creates lower process yields and negatively impacts company profitability?
* Do you know how to create robust and complaint processes?
Areas Covered in the Session\:
* Review the regulatory basis for process validation.
* Understand the difference between Validation and Verification.
* Review IQ\, OQ\, PQ
* Create a robust validation plan using six sigma techniques while maintaining compliance with QSR 820\, ISO 13485\, and GHTF.
* Creating risk classification scheme to help define the rigor of your validation.
* Using risk management at the Qualification stage to assist in revalidation and change control activities while in production.
* Using Risk Management to Maintain a state of control after initial validation is complete.
In 2008\, a new edition of ISO 9001 went into effect. The literature says the new version doesn't introduce any new requirements but only clarifications to the existing requirements.
One of the clarifications involves the use of Outsourced Processes in the Quality Management System. The changes clarify the organization's responsibility for conformity to all customer\, regulatory\, and statutory requirements. The changes reinforce the need for control over outsourced processes and recommend using the methods found in the ISO 9001 Purchasing clause. These changes also include suppliers who are part of the same parent organization\, such as a separate department or division. To help clarify the requirements\, ISO issued a guidance document on Outsourced Processes. The presentation explains the changes to ISO 9001\, and recommendations in the guidance document. We take a practical implementation approach\, showing how to evaluate and select outsource suppliers\, especially service suppliers. We develop methods for written supplier agreements\, which define controls and expectations. A critical element for success is monitoring and measuring of the delivered service. This presentation incorporates supplier scorecards as the most effective tools for this purpose. This webinar explains the changes in ISO 9001\:2008 related to outsourced processes. While the literature says this new version only contains clarifications\, this clarification can have a big impact on a Quality Management System. We look to ISO’s guidance document on outsourced process to ensure we understand the intent.
Why you should attend\: ISO 9001\:2008 clarifies the concept of an outsourced process and expects that you will manage any outsourced process using the purchasing methods in Clause 7.4. The new definition of an outsourced process includes the cases where you obtain a service from your parent company or from a sister division. This broadens the definition to bring in “suppliers” that are not traditional external companies.
Moving the management of outsourced processes to purchasing brings in the concepts of supplier evaluation\, selection\, and monitoring/measuring. This broader definition includes cases without monetary transactions! You will also learn about the ISO guidance document that explains the change in the standard. In addition\, the new concepts mean that you may have a new set of questions (and requests for records) from your ISO 9001 registrar. If your Quality Management System (QMS)\, through its documented procedures\, cannot answer these question quickly\, and without hesitation\, then you\, and your team need to attend this webinar!
* Do you know all the processes required for your quality management system?
* Do you know who performs each process\, i.e.\, can you identify the process owner by job title and name?
* Can you list the QMS processes that you have outsourced?
* Do you have records of the requirements for this supplier\, potential supplier evaluation\, and your selection criteria?
* Can you show how you monitor and measure the QMS process the supplier provides?
* Do you have records monitoring\, measuring\, and feedback for the supplier performing the outsourced process?
Performance-based agency compensation is certainly about paying only for positive results. But it is also about forming long-term\, mutually beneficial client-agency relationships built around common goals.
Date &\; Time-
September 28\, 2010 at 11\:00 AM PDT
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T172159Z DTSTART;VALUE=DATE-TIME:20100928T190000Z DTEND;VALUE=DATE-TIME:20100928T190000Z UID:http://www.webinarcentral.net/content/beyond-stuck-middle-seat%C2%AE-how-disney-lost-then-restored-luster-magic-kingdom URL;VALUE=URI:http://www.webinarcentral.net/content/beyond-stuck-middle-seat%C2%AE-how-disney-lost-then-restored-luster-magic-kingdom SUMMARY:Beyond Stuck in the Middle Seat®\: How Disney Lost\, Then Restored the Luster to the Magic Kingdom DESCRIPTION:What’s the worst place in an airplane? The middle seat! Why? You’re literally stuck in a rotten place\, possibly for a long time\, and you can’t do anything about it. Or can you?
Doug Lipp\, respected author\, speaker and former head of training at Disney University uses the middle seat as a metaphor for what happens to all of us in life ... we get stuck in uncomfortable places. How do you deal with unfortunate situations? When in a situation that you “can’t control\,” what options do you actually have?
This entertaining and thought-provoking webinar will address such topics as\:
* Creative Problem Solving
* Work-Life Balance
* Customer Service
* Product Development
Join us for this fun-filled\, insightful webinar as Doug addresses everything from life-on-the-road horror stories to dealing with organizational change.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T172159Z DTSTART;VALUE=DATE-TIME:20100928T200000Z DTEND;VALUE=DATE-TIME:20100928T200000Z UID:http://www.webinarcentral.net/content/leverage-billing-drive-performance-add-value-your-fsso URL;VALUE=URI:http://www.webinarcentral.net/content/leverage-billing-drive-performance-add-value-your-fsso SUMMARY:Leverage Billing to Drive Performance & Add value to your FSSO DESCRIPTION:Historically\, companies have viewed billing strictly from an operations perspective -- get invoices and statements out the door as efficiently and cost-effectively as possible. But did you realize there are strategic considerations to the billing function as well - ranging from enhanced customer retention\, brand loyalty and cross-selling opportunities along with improved cash flow\, dispute management and customer service? From this perspective\, it's not just about bills going out\; it's also about cash coming in.
Here’s your FREE pass to join an expert panel for an interactive discussion on the operational and strategic benefits of billing. Hear from a panel of experts on how companies are leveraging new billing processes not only to improve their operations but also to support their strategic objectives.
Panel includes\: Tracy Garrett\, Shared Services A/R Manager\, Oldcastle APG
- Rob Hollenbach\, Director Shared Services\, IDEXX Laborato
- Megan Locke\, Credit Supervisor\, Chiquita Brands Int'l
- Mitch Rose\, VP Marketing\, Billtrust
Key topics will include\:
- Paper and electronic bill delivery channels
- Advanced electronic bill delivery channels
- Key factors to consider when outsourcing invoice and statement delivery
- Advanced technology for online invoice presentment and payment
- Operational and strategic benefits of outsourced billing
Legal professionals have to balance the desire for an effective presentation with the need to be more conscious about costs related to the litigation. There is also pressure to be on the cutting edge of courtroom presentation technology. Time and cost constraints also affect the selection and development of demonstrative evidence. The economics of preparing for and trying cases is changing. Our methodology will help in better organizing the visual support of a case by managing expenses at every step of the discovery and trial preparation stage. Participants will learn about the range of methods that are available for presenting the exhibits and supporting visuals that will effectively convey the intended message\, help carry the theme of the case\, and impact the jury so that the intended message will be carried into the jury room.
In this one hour webinar\, you will learn how to\:
1. Look at the case from a visual perspective
2. Better understand how to develop a theme and convert it to an effective message
3. Use a “reverse engineering” approach to developing visual support
4. Find the right balance of media mix and budget
As a bonus\, you will receive\:
Stephen is off ering participants a full case triage review at no charge. This is a $275.00 value. This includes a review of all liability and damages material\, photographs\, radiology\, expert reports\, etc. The participant will receive a written report analyzing the case from a demonstrative perspective\, including suggestions for visual support\, noting any missing material\, and a proposal for the most effective way of presenting the case at mediation\, settlement conference or trial.
Time\: 14\:15 GMT
Being in the Food and/or Beverage industry\, you are under constant pressure\: higher targets\, tougher challenges\, such as broader product variety\, sustainable production processes\, and efficiency\, but not more resources to work with.
So\, how can you keep everyone happy? By converging control\, power\, communications and information technology throughout your plant\, you can move closer to the goal of Plant-wide Optimization.
Participants of this webinar will gain an in-depth understanding on the future of integrated Process Manufacturing Solutions versus a conventional DCS system. Having an integrated solution boosts your profitability by keeping production levels high without endangering personnel\, assets or the environment. You will also get practical guidance on how single platform plant-wide control maximizes productivity\, reduces total cost of ownership\, and minimizes life cycle costs.
Key issues addressed in the session\:
•How can I identify my ENERGY CONSUMPTION and then reduce it?
•How do I know where my COST REDUCTION opportunities reside?
•How do I ENHANCE PERFORMANCE of my existing assets?
Live Q&\;A with your hosts
Have your Plant Optimisation questions answered by leading industry experts. Please submit your question today via the registration form.
The speaker\: Paul Greene is the Business Manager for Consumer Goods and Process Technologies with Rockwell Automation Global Solutions. Paul has 20 years of experience delivering automation and information solutions in manufacturing.
Intended audience\: Plant Managers\, Directors of Supply Chain\, Operations\, Innovation\, Research and Development\, and Quality in the Food &\; Beverage sector.
Technical Requirements
- PC headset
- PC speakers
- Broadband Connection
This course provides a comprehensive review of Good Clinical Practice (GCP) and FDA regulations and requirements.
Participants receive a foundation of knowledge about GCP\, practical examples\, and the underlying scientific and regulatory principles involved. Guidelines for each aspect of research are provided\, as well as information on the structuring and preparation of protocols\, consent forms\, and investigator brochure. Information on maintaining ongoing compliance will also be discussed. This course enables clinical professionals to prepare concise documents and provide their company and the FDA with necessary information for their clinical studies.
Areas Covered in the Session\:
* Discuss the FDA's role in Drug Development
* Principles of GCP
* Activities that are common to most trials
* Summarize FDA GCP regulations
* Recognize how GCP impacts the clinical research process
* Prepare concise documents and provide
* Necessary information for clinical studies compliance
* Maintain ongoing compliance
Who Will Benefit\: This webinar will provide valuable assistance to all personnel in\: Pharmaceutical\, Biotechnology\, CROs and Research Facilities Conducting Clinical Trials including\:
* Managers in Clinical Development and Project Leaders
* Quality Assurance Managers and auditors
* Clinical Research Associates
* Clinical Operations Staff
* Regulatory Compliance Associates and Managers
Learn how to monitor and track cash flow for your small business.
What would you do if your company ran out of cash tomorrow? Businesses can show a profit on their financial statements….but still fail due to lack of cash flow. Take control now. Don’t be forced to close your doors and join the ranks of the unemployed.
Daryl Murrow\, a business owner for nearly two decades and cash flow management expert\, helps small business owners take control of their financial situation and make better decisions. Daryl provides you with the cash flow insight you need to keep your business solvent and successful.
You will learn how to\:
* Utilize the Cash Flow Analysis Tool that can be modified to fit your business cash flow needs.
* Quickly forecast income and expenses on a weekly basis.
* Recognize unwanted cash surprises before they occur.
* Improve your decision making by always knowing your cash position.
* Be in control of your most important liquid asset\, CASH.
All registrants also receive\:
* A handout for use during the webinar
* Weekly Cash Flow Analysis Tool
* A recording of the class available for 30 days.
As an added bonus\, the first 50 registrants receive our report\, “Cash Flow Strategies for the Small Business Owner” to help you implement the teachings from the eLearning training course.
Suggested Attendees\: Small Business Owners\, Finance Managers
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T172159Z DTSTART;VALUE=DATE-TIME:20100929T170000Z DTEND;VALUE=DATE-TIME:20100929T180000Z UID:http://www.webinarcentral.net/content/webinar-sep-292010-business-continuity-virtualization URL;VALUE=URI:http://www.webinarcentral.net/content/webinar-sep-292010-business-continuity-virtualization SUMMARY:Webinar on Sep 29\,2010 - Business Continuity with Virtualization DESCRIPTION:Most IT managers are continuing to look for ways to save money in the IT enterprise. One of the chief concerns for IT professionals is implementing a Business Continuity/Disaster Recovery solution. This webinar is designed to show you how to manage Business Continuity with Virtualization.
Raj Kosuri\, CTO and Terell Jones Director of Infrastructure for Ecomnets\, the industry's leading authorities on Green IT infrastructure design and management will discuss\:
• Why use virtualization as a business continuity strategy?
• How does it maximize performance?
• How does it minimize TCO?
Who Should Attend\: Professionals new to virtualization including\: CEO\, CIO\, CTO\, CFO\, CSO\, COO\, IT Managers\, Data Center Managers\, Facilities Managers\, Business Managers
About EcomNets\:
EcomNets Green IT Solutions can help you save energy costs\, save cooling costs\, and reduce your carbon footprint. EcomNets are experts in PC Power Management\, Virtualization\, Cloud Computing\, Data Center Best Practices\, and Electronic Waste Management. EcomNets can help you easily develop a Green IT strategy compatible with your business processes. EcomNets Green IT Solutions delivers fast\, flexible\, and affordable solutions\, helping you drive consistent and measurable improvements in your Green IT Initiatives.
Register for a session now by checking a date below\:
Wed\, Sep 29\, 2010 11\:00 AM - 12\:00 PM EDT
https\://www1.gotomeeting.com/register/726621008
Wed\, Oct 27\, 2010 11\:00 AM - 12\:00 PM EDT
https\://www1.gotomeeting.com/register/238994081
Wed\, Dec 1\, 2010 11\:00 AM - 12\:00 PM EST
https\://www1.gotomeeting.com/register/869060065
Wed\, Jan 12\, 2011 11\:00 AM - 12\:00 PM EST
https\://www1.gotomeeting.com/register/210026305
Once registered you will receive an email confirming your registration with information you need to join the Webinar.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T172159Z DTSTART;VALUE=DATE-TIME:20100929T190000Z DTEND;VALUE=DATE-TIME:20100929T190000Z UID:http://www.webinarcentral.net/content/free-webinar-planning-your-first-webinar-1 URL;VALUE=URI:http://www.webinarcentral.net/content/free-webinar-planning-your-first-webinar-1 SUMMARY:FREE Webinar\: Planning Your First Webinar DESCRIPTION:Planning Your First Webinar
~The What\, Why and How to Make it a Success
This webinar is appropriate for those wanting a basic understanding of the mechanics of delivering a webinar. It is valuable for those considering using webinars to deliver educational programming and for those just getting started with webinars as a new marketing channel.
What You Will Learn\:
• Each step in the webinar planning process - Identify all of the elements needed - from speaker selection to post-event follow-up - to produce professional webinars.
• Guidelines to evaluating vendor options - Learn the differences between webinar technology providers.
• Simple marketing tasks that drive webinar attendance - Discover the latest techniques to find and market to your audience.
What You Will Get\:
• A FREE \\"Planning a Successful Webinar\\" e-kit
• A LIVE question and answer session
About the Presenter\:
Don Cameron\, Marketing Strategist and founder of Interactive Telesis and ConferTel\, has helped hundreds of organizations generate non-dues revenue by delivering educational webinars to their members in addition to helping businesses use an educational marketing approach to cost-effectively generate qualified sales leads.
Time\: 14\:15 GMT
Intended to consolidate discrimination legislation\, the Equality Act 2010 will have significant implications for employers. In this webinar Capital Law will help delegates understand the key principles and obligations of the act focusing particularly on the following\:
•New rules on dual\, associative and perceived discrimination
•Changes to the scope of disability discrimination
•Extension of third party harassment and employer's liability for other people's actions
•Changes to equal pay law
•New public sector equality duty
From this session you can expect to learn\:
•Practical implications of the change to equality legislation that this act represents
•How employers should discharge their new responsibilities under the act in the most straightforward and cost effective way
•Pre-employment questionnaires\, friend or foe?
The speakers\: Elin Pinnell\, Partner\, Head of Employment Law\, Capital Law LLP. Elin regularly trains client companies in employment law and HR issues. She also advises behind the scenes in contractual disputes\, disciplinary matters\, redundancies and re-organisations\, as well as representing clients at tribunals across the UK.
Henry Gilbert\, MD &\; Lead Consultant\, Holistic Services Limited. Henry Gilbert is an HR professional with Board level experience with responsibility for HR\, Purchasing &\; Supply. He is an experienced advocate in Employment Tribunals and is a Council Representative for the Chartered Institute of Personnel and Development.
Intended audience\: HR Directors and Managers\, Senior Legal HR Advisors\, Employee Relations Directors\, HR Officers\, and those involved in legal HR issues.
Technical Requirements
- PC headset
- PC speakers
- Broadband Connection
The FDA regulations contain a vast quantity of requirements\, which govern tasks performed by your company's personnel every day.
Are there going to be noncompliance? You bet. Are you going to correct these noncompliances? Only if you identify them. To ensure substantial compliance\, your company needs an effective audit program for both internal and external processes. To have an effective audit program\, your company needs an effective audit team. This session will detail the best methods or training auditors\, and include the best methods for performing internal audits as well as audits of suppliers and subcontractors.
Areas Covered in the Session\:
* Effective Methods for auditor training.
* Establishment of an internal audit program.
* How to perform internal audits to maximize results
* Establishment of an \\"external\\" audit program.
* How to perform supplier/contractor audits to improve business relationships
Who Will Benefit\: This webinar will provide valuable assistance to all regulated companies\, since internal and external auditing are requirements across the Medical Device\, Diagnostic\, Pharmaceutical\, and Biologics fields. The employees who will benefit include\:
* Executive/senior management
* Regulatory management
* QA management
* Purchasing management
* Quality system auditors
Talend\, the recognized market leader in open source data management software\, and Netezza Corporation\, the global leader in data warehouse\, analytic and monitoring appliances\, have joined in a partnership to deliver combined data management solutions.
As part of this partnership\, Talend and Netezza have developed a certified integration solution that combines Talend's unmatched open source data management products and the price/performance-leading Netezza TwinFin data warehouse appliance. All the Talend connectors on Netezza are certified for Netezza 5.0.
This one hour webinar will show how to\:
- Connect\, read and write on a database table
- Streamline and reduce the complexity of critical data management projects resulting in higher productivity\, lower operational costs and greater insights into vital informational assets
- Create slowly changing dimensions
- Load data in bulk mode
A demonstration of several concrete cases will also be presented in this webinar.
When\: September 30th at 10am BST
Sign up here\: http\://nxy.in/5j2lh
“Application Retirement is emerging as a structured approach in application portfolio management. The costs associated with managing legacy applications can be significant – organizations must maintain expensive application operating environments simply because they need to retain application data. Extracting data from legacy applications in a simple and straightforward way while ensuring access to this data over time allows organizations to reduce costs and ensure compliance.” - Sheila Childs\, Gartner’s Research Director of Storage Technologies and Strategies
Solix ExAPPS Industry's first Application Retirement appliance - is pre-built\, pre-configured\, pre-tested with all necessary software and hardware components - introduces simplicity to a complex problem. Customers with finite number of specific packaged and custom applications on distributed systems will find the appliance most appealing as it will allow automated repeatable process for multiple applications
During this webinar\, you will learn how Solix ExAPPS - Industry's first Application Retirement Appliance - will help organizations to get a jump start on Application Retirement projects
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T172159Z DTSTART;VALUE=DATE-TIME:20101005T180000Z DTEND;VALUE=DATE-TIME:20101005T190000Z UID:http://www.webinarcentral.net/content/fda-tripod-clinical-trial-regulations-compliance-and-gcp-drug-development URL;VALUE=URI:http://www.webinarcentral.net/content/fda-tripod-clinical-trial-regulations-compliance-and-gcp-drug-development SUMMARY:The FDA Tripod - Clinical Trial Regulations\, Compliance and GCP in Drug Development DESCRIPTION:This GCP training Webinar will discuss the principals of GCP\, the regulations pertaining to it and elements necessary for FDA compliance.
Why Should You Attend\:
This course provides a comprehensive review of Good Clinical Practice (GCP) and FDA regulations and requirements. Participants receive a foundation of knowledge about GCP\, practical examples\, and the underlying scientific and regulatory principles involved. Guidelines for each aspect of research are provided\, as well as information on the structuring and preparation of protocols\, consent forms\, and investigator brochure. Information on maintaining ongoing compliance will also be discussed. This course enables clinical professionals to prepare concise documents and provide their company and the FDA with necessary information for their clinical studies.
Areas Covered in the Seminar \:
Time\: 14\:15 GMT
Only 30% of Change programmes are successful\, according to a survey of business executives by McKinsey &\; Company in 2008.
This webinar will highlight the change management themes that make the difference between success and failure. It will also demonstrate how these play a pivotal role in helping organisations\, wherever they are on the change journey or the size of the change programme\, to manage change successfully and to deliver a positive return on investment.
You will discover how to\:
•Increase your chances of success - by continuously focussing on outcomes
•Achieve success at whatever stage you are at in the change journey
•Identify and mitigate common risks - by working collaboratively with others
•Measure the change that you visualised at the outset
The presentation will include real examples of the above\, based on practical experience\, as well as pragmatic guidance that can increase your organisation’s chances of success.
This session will be followed by live Q&\;A with the hosts including\:
Fay Thompson\, HR Director
Keith Baker\, Business Transformation Specialist
David Knowles-Leak\, Leadership &\; Business Transformation Specialist
The Q&\;A will be moderated by David Strong\, Managing Director of A2Z HR Solutions.
Intended audience\: HR Directors and Managers\, Recruitment Managers\, HR Project Managers\, Training and Development Managers\, and those working in areas of Leadership and Business Change
Technical Requirements
- PC headset
- PC speakers
- Broadband Connection
NorthgateArinso and SAP invite you to a 60-minute Virtual Briefing about Integrated Talent Management.
During this interactive webinar\, you will discover how integrated talent management supports the process of finding\, nurturing\, rewarding and retaining the best people and talent within your organization\, through integrating HR processes.
A panel of HR experts will explain why integration really matters. Weaving individual Talent Management processes together into a consolidated system will let you uncover the benefits of enterprise-wide talent management\, such as\:
- How performance management can help optimize compensation planning
- How succession planning helps you to educate &\; develop future leaders by learning
- How global HR administration and data management leverages your HR investment across all Talent Management processes
PLUS\: Enjoy a live demo of how euHReka handles key transactions in HR administration\, payroll and talent management in an intuitive\, fast\, flexible and smartly integrated way.
What's in it for you?
- Learn more about the added value of integrated Talent Management
- Observe how easy it is to efficiently manage the life-cycle of your workforce
- Participate in a global forum and interact with fellow HR/IT decision makers and subject matter experts
Let us show you what our Trading Education do can for you!
The FREE 60 minute Webinar was created to assist traders (beginner\, novice and expert) from around the world in their quest to trade Forex and Futures. We understand the statement – \\"No one is born a trader\, it takes an education.\\" We have an entire education system to get you up to speed quickly. Our comprehensive trading education includes our proven money making strategies\, 24 hour live trade rooms\, live classrooms 6 days a week\, 1-on-1 coaching and much more.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T172159Z DTSTART;VALUE=DATE-TIME:20101007T095200Z DTEND;VALUE=DATE-TIME:20020203 UID:http://www.webinarcentral.net/content/how-can-plm-support-your-business URL;VALUE=URI:http://www.webinarcentral.net/content/how-can-plm-support-your-business SUMMARY:How can PLM support your business? DESCRIPTION:Time\: 14\:15 GMT
PLM has evolved.....
What does this mean for your business?
Join us at this one hour live webinar and find out.
PLM has moved away from the traditional role of engineering data management is now considered a total strategic business support\, capable of unlocking information and disseminating across the entire value chain.
During this one hour long live webinar we will be looking at\:
•Core drivers of efficient PLM
•The areas where PLM can make a difference within the business environment
•The prerequisites to an efficient PLM platform
•Practical examples that underpin the above bullets
The potential of PLM is enormous\, join us to discover how it can\:
•Support all business processes
•Help manage complex environments
•Help improve productivity
•Support collaboration
This webinar will be followed by a live Q&\;A session with your host. Submit your questions today via the registration form.
Technical Requirements
- PC headset
- PC speakers
- Broadband Connection
Intended audience\: Directors of Supply Chain\, Operations\, Innovation\, Research and Development\, and Quality\, Plant Managers
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T172159Z DTSTART;VALUE=DATE-TIME:20101007T190000Z DTEND;VALUE=DATE-TIME:20101007T190000Z UID:http://www.webinarcentral.net/content/aggregate-spend-disclosure-turn-stress-success URL;VALUE=URI:http://www.webinarcentral.net/content/aggregate-spend-disclosure-turn-stress-success SUMMARY:Aggregate Spend Disclosure\: Turn Stress into Success DESCRIPTION:An ever increasing number of states and the federal government have existing or pending regulations for collecting\, managing\, and reporting of spend. With rules that vary by minimum disclosure amounts\, deadlines\, and penalties\, aggregate spend reporting can present significant operational challenges.
In this session\, you'll\:
- Learn about the risks and rewards of several common strategies employed for aggregate spend reporting
- Hear compelling real-life scenarios that illustrate the benefit of incorporating customer master and data enrichment environments into aggregate spend solutions
- Review available technology systems and solutions designed to meet the challenges posed by aggregate spend reporting
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T172159Z DTSTART;VALUE=DATE-TIME:20101011T103800Z DTEND;VALUE=DATE-TIME:20020203 UID:http://www.webinarcentral.net/content/ondemand-webinar-building-business-case-database-archiving URL;VALUE=URI:http://www.webinarcentral.net/content/ondemand-webinar-building-business-case-database-archiving SUMMARY:OnDemand Webinar\: Building the Business Case for Database Archiving DESCRIPTION:This Presentation covers the three essential ingredients of any business case for implementing database archiving functionality for an existing database application
* Cost reduction
* Productivity improvements
* Risk reduction
This Webcast shows how to compute the value for operational applications\, for retired applications\, and for using database archiving as part of an application renovation project. It also includes a list of participants who should be working together as a team to determine the worth of such projects.
During this webinar\, you will learn how database archiving\, when applied properly to an appropriate application can return huge value and reach ROI in a very short time.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T172159Z DTSTART;VALUE=DATE-TIME:20101012T190000Z DTEND;VALUE=DATE-TIME:20101012T190000Z UID:http://www.webinarcentral.net/content/stop-looking-marketing-and-sales-results-all-wrong-places URL;VALUE=URI:http://www.webinarcentral.net/content/stop-looking-marketing-and-sales-results-all-wrong-places SUMMARY:Stop Looking for Marketing and Sales Results in all the Wrong Places DESCRIPTION:Sales and Marketing alignment continues to be a major concern for top management\, especially when company survival in a tough economic climate depends on the efficiency and effectiveness of its revenue engine. Many companies have tried to align Sales and Marketing using re-organization\, new hires\, training\, team-building exercises\, and technology. Typically\, the results are less than spectacular and are short-lived.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T172159Z DTSTART;VALUE=DATE-TIME:20101012T183000Z DTEND;VALUE=DATE-TIME:20101012T183000Z UID:http://www.webinarcentral.net/content/how-best-became-best-online-video-advertising URL;VALUE=URI:http://www.webinarcentral.net/content/how-best-became-best-online-video-advertising SUMMARY:How the Best Became the Best in Online Video Advertising DESCRIPTION:Old Spice\, Evian\, and BlendTec have created the most-watched online video ads of all-time. But how did they do it? Using its industry-wide data set from the world of online video advertising\, Visible Measures will share exclusive insights and best practices that enabled these campaigns to become the most-watched in history. If you're looking to increase your campaign performance in online video\, this is a webinar you won't want to miss.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T172159Z DTSTART;VALUE=DATE-TIME:20101013T084000Z DTEND;VALUE=DATE-TIME:20020203 UID:http://www.webinarcentral.net/content/what-every-leader-can-learn-successful-new-ceos URL;VALUE=URI:http://www.webinarcentral.net/content/what-every-leader-can-learn-successful-new-ceos SUMMARY:What Every Leader Can Learn from Successful New CEO's DESCRIPTION:Time\: 15\:15 GMT
This webinar is part of the Leading Minds Series ‘Taking Charge\: Leadership and Success’
Learn from the globally renowned expert about the \\"best practices\\" for new CEO's to apply\, and some of the all important 'do's &\; don'ts' for people who take up leadership positions lower in the organisation.
We'll look first at what works for CEO's - and then say\, well\, wait\, what about the rest of us\, as we take the reins? At lower levels there may inherently be more emphasis on great project management and compelling analytics vs direction setting. People who lead at lower levels may have less ability to pick and shape their team (certainly their peers) than CEO's.
This 60 minute live session will give you an insight into Tom's current project and is a must attend for established business leaders and also those aspiring to be.
About the speaker\: Thomas A. Stewart is the Chief Marketing and Knowledge Officer (CMKO) of the global management consulting firm Booz &\; Company.
Stewart most recently served as editor and managing director of Harvard Business Review\, and is a best-selling author\, an authority on intellectual capital and knowledge management\, and an influential thought leader on global management issues and ideas.
Register now and submit your questions to be answered live by Tom Stewart during the Q&\;A session.
Price\: £50 ($80)
Technical Requirements
- PC headset
- PC speakers
- Broadband Connection
Purchase to Pay Automation\: Goals and challenges in a global enterprise
Effective change management is key to the success of any project which alters the way people work\; whether that be a change to processes\, technologies\, systems or structures. However\, many projects still suffer when organizational issues aren’t adequately addressed\; so what practical steps can you make within your project delivery to ensure success and achieve your goals?
Nigel Chapman\, Change Management Facilitator at ABB\, will deliver a case study and share his experience and practical advice\, providing you with key steps to reduce project risk and attain faster ROI. ABB successfully automated their invoice processing to increase efficiency and reduce costs. Join this webinar to find out how ABB successfully reaped the best results from their P2P automation program and discover\:
- How to manage change regionally in line with the global enterprise
- Ways to gain stakeholder interest and developing user commitment
- How to achieve process centralization and system integration
- Techniques for tackling non-compliance
- A path to determine project success
- The top 5 lessons learnt and success factors from the UK regional implementation
Generate Revenue with Webinars
~Discover a New Way to Earn Profit
Whether you are looking to earn non-dues revenue or create an additional income source\, offering paid webinars is an easy way to profit from your knowledge. This webinar explores ways to best convert your valuable\, industry-specific knowledge into something tangible – and profit from it.
What You Will Learn\:
• Various types of revenue generating webinars
• Tips to create value from content
• Marketing techniques to attract audiences
• Components required to offer CEU credits
Who Should Attend\:
• Professionals who wish to leverage their industry knowledge for profit
• Association Executives who are looking to earn non-dues revenue
• Anyone who has access to content that is valuable to others
All Attendees will receive\: a copy of \\"Costs of Putting Together a Webinar”
About the Presenter\:
Don Cameron\, Marketing Strategist and founder of Interactive Telesis and ConferTel\, has helped hundreds of organizations generate non-dues revenue by delivering educational webinars to their members in addition to helping businesses use an educational marketing approach to cost-effectively generate qualified sales leads.
You would like to implement MDM into your corporate IT systems\, but how? Is your database going to fit in this new application? What does it entail? What are the advantages of such a solution? All the answers to your questions are in this webinar.
This 50 minute live webinar will present\:
- How to connect to multiple sources and combine it into a single Repository
- How to synchronize data (web services\, flat files\, BAPI\, etc.) and distribute the data to various systems (SAP\, SQL\, flat files\, databases etc.)
- How to ensure security across these platforms
- How to combine Master Data Governance with data enrichment and data profiling
A demonstration of a Talend customer use case will be shown. A question and answer session will be organized to allow you to make every last doubt disappear.
Date\: October 14th
Time\: 10am BGT
Sign up now\: http\://nxy.in/tixyj
The PRSA 2010 Conference in Washington DC this coming October 16-19th features keynote presentations from some of the most influential and respected thought leaders of social technology\, online research\, branding\, crisis communications and public affairs.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T172159Z DTSTART;VALUE=DATE-TIME:20101020T091100Z DTEND;VALUE=DATE-TIME:20020203 UID:http://www.webinarcentral.net/content/new-steps-innovative-electronic-batch-recording URL;VALUE=URI:http://www.webinarcentral.net/content/new-steps-innovative-electronic-batch-recording SUMMARY:New Steps to Innovative Electronic Batch Recording DESCRIPTION:Time\: 14\:15 GMT
For years Electronic Batch Recording (EBR) systems tried to mimic paper based batch records. Rockwell Automation broke with the old ‘Paper- On-Glass’ paradigm to help maximise productivity of every user at every step of the lifecycle from recipe design to execution\, review and approval.
The webinar will explore a new way to implementing MES in the pharmaceutical industry with a case study from F. Hoffmann - La Roche AG
Learn how F. Hoffmann - La Roche AG successfully implemented a new MES in their pharmaceutical drug substance production. Mr. Robert Fretz\, Head of Process Automation and MES\, will talk about the benefits of a new MES solution\, especially\, an innovative integration scenario within the heterogeneous DCS landscape.
Additionally Martin Dittmer\, Product Manager at Rockwell Automation will explain major MES concepts\, and give a live demonstration with the system\, giving an insight into excellent usability and look and feel.
This webinar will help you to
•Understand how to minimise time and cost for MES integration
•Understand how to increase 'right first time' on the shop floor
•Understand how to create master recipes faster
Intended audience\: CEO’s\, CIO’s\, plant directors\, quality directors\, production directors and compliance officers in drug manufacturing\, biotech\, and API sectors of the pharma industry
Technical Requirements
- PC headset
- PC speakers
- Broadband Connection
“On average 10% of applications in an unoptimized portfolio are candidates for retirement. An additional one-third can require migration or rationalization”. - Jim Duggan\, Gartner analyst (Plan Legacy Application Retirements carefully\, April 2009)
Application Retirement is part of Application Portfolio Management that must be undertaken on a continuing basis since applications often outlive their usefulness. However\, one may need to retain and manage legacy data from such applications which are candidates for retirement.
During this webinar\, you will learn how Solix EDMS Application Retirement along with Solix Application Retirement Managed Services can help organizations
* Target which applications to retire
* Decide which data to keep\, for how long and for what purpose (compliance\, litigation support\, records management or business operations)
* Determine the access requirements
* Determine the optimal secure platform to retain such legacy data\; and finally
* Calculate the benefits of retirement
Application Retirement is essentially about reducing costs\: of hardware/software AMC\, and people trained on legacy systems.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T172159Z DTSTART;VALUE=DATE-TIME:20101021T090100Z DTEND;VALUE=DATE-TIME:20020203 UID:http://www.webinarcentral.net/content/unique-approach-ensuring-food-safety-manage-contamination-not-recalls%E2%84%A2 URL;VALUE=URI:http://www.webinarcentral.net/content/unique-approach-ensuring-food-safety-manage-contamination-not-recalls%E2%84%A2 SUMMARY:A Unique Approach for Ensuring Food Safety - Manage Contamination not Recalls™ DESCRIPTION:Time\: 16\:15 BST
Contamination with chemical or biological adulterants can occur from natural\, accidental or intentional events however effective detection is paramount. An integrated approach encompassing collection\, sampling\, sample preparation\, detection and tracking will be described offering a unified holistic approach to managing contamination.
Participants will learn about new technologies which can help food commodity suppliers and food processors manage contamination in a timely and cost effective manner and help reduce or eliminate costly recalls.
Webinar attendees will explore\:
•Sampling of dry goods\, fluids and surfaces
•New biosensor approaches
•A secure web-based tracking tool enabling farm-to-table view for contamination monitoring
•Which contaminants need to be monitored to ensure a holistic food safety protocol exploring bacteriological types and strains
Key issues addressed\:
•Importance of managing contamination before products enter the food supply chain
•Sampling and collection is critical to an effective contamination detection strategy
•Unique detection strategies enable timely\, specific and cost effective food protection
•Importance of a complete a contamination portfolio - biological strain
Register now and submit your food safety questions to be answered live\, go to
http\://www.wtgwebinar.com/webinar/a-unique-approach-for-ensuring-food-safety---manage-contamination-not-recalls™/139
Intended Audience\: Senior level managers and Directors responsible for food safety and/or QA/QC within food or beverage manufacturing industry
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T172159Z DTSTART;VALUE=DATE-TIME:20101021T090000Z DTEND;VALUE=DATE-TIME:20101021T090000Z UID:http://www.webinarcentral.net/content/construire-un-mod%C3%A8le-de-donn%C3%A9es-mdm-%C3%A0-partir-de-z%C3%A9ro URL;VALUE=URI:http://www.webinarcentral.net/content/construire-un-mod%C3%A8le-de-donn%C3%A9es-mdm-%C3%A0-partir-de-z%C3%A9ro SUMMARY:Construire un modèle de données MDM à partir de zéro DESCRIPTION:Ce tutoriel live de 45 minutes vous présentera\:
- Comment configurer un conteneur de données
- Comment définir et créer un modèle de données
- Comment créer des vues de navigation correspondant au modèle de données
- Comment visualiser les changements dynamiques du modèle
Une démonstration de plusieurs cas concrets sera également proposée au cours du tutoriel.
Pour vous inscrire à ce tutoriel live gratuit \: http\://nxy.in/37cig
Date \: 21 octobre 2010
Horaire \: de 10h à 12h CET
QuickBooks Friday Free For All Support Webinar
What do you want to know?
Here's your chance to ask your QuickBooks accounting questions. There is no charge to attend and no travel involved - all you need is computer with an internet connection and speakers. Voice access with a telephone or computer microphone are optional.
How it works\:
You ask the questions\, we answer &\; demonstrate the steps involved via webinar. We take questions in the order guests arrive to the sessuib. Once everyone has had 1 question answered\, we continue around the room again starting with the first guest. We repeat the process as time permits.
How we ask &\; answer questions\:
Computer only - Use the training system's chat window to ask your questions. Listen through your computer speakers while you watch the live demonstration of each answer on your computer.
or
Computer with microphone - Ask your questions using your computer's microphone. Listen through your computer speakers while you watch the live demonstration of each answer on your computer. (Microphone sound quality varies greatly and cannot be guaranteed.)
or
Computer and telephone - Call into the phone conference (toll charges may apply). Ask your questions and hear the answers over the phone while you watch the live demonstration of each answer on your computer.
We appreciate your participation and feedback.
Feel free to suggest specific topics for a meeting by e-mailing Training@AccountingMadeSimple.biz
We look forward to seeing you soon!
Anna Sheets
Certfied QuickBooks ProAdvisor
Certified QuickBooks Point of Sale ProAdvisor
Group Facilitator &\; Presenter
Sponsored by\:
Accounting Made Simple
QuickBooks Training &\; Optimization Pros
www.AccountingMadeSimple.biz
This webcast will focus on protecting data assets in enterprises while at the same time ensuring referential integrity for application testing using comprehensive data management strategy. As data in enterprises keep growing
* the costs for storage and IT resources keep increasing for application testing as well\;
* it exposes enterprises to a constant risk of data privacy regulations.
In this session we will see how Solix Enterprise Data Management Suite (Solix EDMS) provides secure and rapid application testing that is built in partnership with Oracle and a seamless end-to-end integrated model for database subsetting\, cloning and masking.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T172159Z DTSTART;VALUE=DATE-TIME:20101026T092800Z DTEND;VALUE=DATE-TIME:20020203 UID:http://www.webinarcentral.net/content/addressing-corrosion-existing-pressure-equipment URL;VALUE=URI:http://www.webinarcentral.net/content/addressing-corrosion-existing-pressure-equipment SUMMARY:Addressing corrosion on existing pressure equipment DESCRIPTION:Time\: 14\:15 GMT
The majority of conventional maintenance is executed under a long term contract with a general contractor\, who provides a wide range of services\, fixing nearly all common repairs. However a few problems can only be fixed using a specialty high risk solution and that is where technology can bring value. Equipment upgrades also exceed maintenance services and require engineering support to define the best design\: metallurgists\, corrosion experts\, FEA experts\, welding engineers but also tooling engineering capacity.
Through a risk analysis process we can propose a technology based safer solution and provide a long term improvement on the critical corrosion issue of major components\: safety in design\, safety in execution\, safety in service operation.
Featured case study\:
A recently executed project with the most recent overlay technology used in situ on a distillation column suffering from corrosion on the shell. The specificity of this project is that another area of the same column was also suffering from corrosion and the shell has been replaced by windows in parallel with the overlay during the same turnaround.
The different steps of this project will be explained\:
•Identification of the corrosion
•Selection of repair solution
•Selection of metallurgy
•Execution and safety
What will I learn?
•How technology can be utilised to repair and improve the reliability of existing major pressure and mechanical equipments
•Assess alternative solutions to the traditional maintenance approach and even more interesting solutions instead of replacing existing equipments due to process changes
•Optimise investment and improve the performance of production tools through innovating technology
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T172159Z DTSTART;VALUE=DATE-TIME:20101026T180000Z DTEND;VALUE=DATE-TIME:20101027T010000Z UID:http://www.webinarcentral.net/content/full-day-virtual-seminar-design-and-validation-excel-spreadsheets-step-step-webinar-complian URL;VALUE=URI:http://www.webinarcentral.net/content/full-day-virtual-seminar-design-and-validation-excel-spreadsheets-step-step-webinar-complian SUMMARY:Full Day Virtual Seminar - Design and Validation of Excel Spreadsheets\: Step-by-Step - Webinar By ComplianceOnline DESCRIPTION: \;In this excel \;Spreadsheet \;validation full day webinar training\, learn the best way to design and validate the excel spreadsheets. Learn what the requirements are of excel validation and how to implement it to comply with regulations.
\;
Why Should You Attend\:
Excel spreadsheets used in regulated environments should be validated and comply with other FDA requirements. In this interactive one-day on-line seminar Dr. Ludwig Huber will give an introduction to FDA\, GAMP®\; 5 and other requirements for validation of excel sheet and present approaches for implementation. This is a comprehensive course covering validation\, design\, testing of functions along with how to apply risk based validation techniques for spreadsheet application. Learn best practices of document planning\, specifications\, installation\, testing and changes.
Learning Objectives\:
How It Works\:
This excel validation virtual event has 6 modules. Our speaker will deliver the modules using PowerPoint slides. Practical examples\, case studies and exercises will be dispersed into and between the presentations. About 50% of the time will be dedicated to discussions and practical sessions. As an example\, attendees will receive fill-in templates to document validation steps from beginning to end\, in other words\, from validation planning and writing specifications to testing and writing the validation report. Application examples will be generic and easy to understand. The results will be discussed and conclusions will be documented by the presenter and will be available for download from a special reference website. Attendees can use the templates to validate and document their own Excel applications. At the end of each module participants can ask verbal questions through the audio line. Written questions can be submitted at any time.
\;
\;This drug safety training will discuss the various factors to be considered and the principles of risk assessment to be followed during drug development to minimize risk.
\;
Areas Covered in the Seminar\:
Who Will Benefit\: \;The Webinar will present valuable risk management information and provide a familiarity with practices to mitigate risk by pharmaceutical and biotechnology personnel involved in drug development\, including\:
\;
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T172159Z DTSTART;VALUE=DATE-TIME:20101026T190000Z DTEND;VALUE=DATE-TIME:20101026T195000Z UID:http://www.webinarcentral.net/content/basics-1031-tax-deferred-exchange-0 URL;VALUE=URI:http://www.webinarcentral.net/content/basics-1031-tax-deferred-exchange-0 SUMMARY:The Basics of the 1031 Tax-Deferred Exchange DESCRIPTION:This webinar will discuss the basics of the 1031 exchange process. Topics will include\:
- Definition of a 1031 Exchange
- Like-Kind Defined
- Capital Gains &\; Boot
- Completing a successful 1031 Exchange
- Timeframes in a 1031 Exchange
- Selecting a Qualified Intermediary
The audio portion of the webinar will be broadcast over your computer's speakers and via telephone. You may choose to call in and ask questions or you may listen to the webinar over the internet and enter questions via text.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T172159Z DTSTART;VALUE=DATE-TIME:20101026T180000Z DTEND;VALUE=DATE-TIME:20101026T180000Z UID:http://www.webinarcentral.net/content/how-treat-adult-children-divorce-acod-preventing-mistakes-and-repairing-damage-1 URL;VALUE=URI:http://www.webinarcentral.net/content/how-treat-adult-children-divorce-acod-preventing-mistakes-and-repairing-damage-1 SUMMARY:How to Treat Adult Children of Divorce (ACOD)\: Preventing Mistakes and Repairing the Damage DESCRIPTION:Post-divorce adjustment for adolescents and young adults facing the separation of their parents is both a surrealistic and confusing time. Family permanence shatters\, the covenant of safety ends\, feelings of victimization and abandonment intensify\, and the expected new role of the offspring forces unwanted changes. As survivors\, they become Adult Children of Divorce (ACOD). This workshop addresses this population’s self-defeating reactions to the initial shock and residual effects of divorce. It shows the productive steps available for better self-control and family reconciliation through evidence-based\, behaviorally-based interventions that guide the ACOD into a transition of accepting and adopting healthier perspectives of their parents and selves.
What you will learn\:
Examine the common problems adolescents and young adults experience when their parents divorce.
Describe the emotional and behavioral self-defeating side-effects of passive-aggressiveness.
Discover four easily implemented methods to reverse the ACOD’s thinking and restore familiar\, positive\, pre-divorce behavior patterns.
Technical requirements\:
To view this webinar you will need to download the WebEx Application. You will be prompted to download it when you first enter the site. To save time\, you can setup prior to the meeting by following this link\: https\://apidemoeu.webex.com/apidemoeu/meetingcenter/mcsetup.php
Disclaimer\:
This event qualifies for one CE credit. Only registered attendees will have access to CE. A Cross Country Education web account is required to attend. There is no charge for a CCE web account. It is recommended that you join the meeting 15 to 20 minutes early. Speaker phone sound quality is poor and it is recommended that they not be used to listen to the event.
\;This pharma training will discuss how to monitor impurities in pharmaceutical products as per ICH Q3 A/B requirements and learn how to measure the thresholds to report for regulatory submission.
\;
Learning Objectives\:
Upon completion of this session\, attendees will understand regulatory requirements in the monitoring of pharmaceutical impurities. Participants will gain practical knowledge about key considerations when reporting impurities for regulatory submission. This session will also discuss observations and infractions that were obtained due to recoding impurities in pharmaceutical labs.
Areas Covered in the Seminar\:
Who Will Benefit\:
To get the most out of the course\, we highly recommended that you have at least two years of pharmaceutical analysis or drug development experience.
\;
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T172159Z DTSTART;VALUE=DATE-TIME:20101027T180000Z DTEND;VALUE=DATE-TIME:20101027T190000Z UID:http://www.webinarcentral.net/content/case-social-media-management-and-archiving URL;VALUE=URI:http://www.webinarcentral.net/content/case-social-media-management-and-archiving SUMMARY:The Case for Social Media Management and Archiving DESCRIPTION:A live Webinar sponsored by FaceTime\, Smarsh and Messaging News
Date &\; Time\:
Wednesday\, October 27\, 2010
1\:00pm EDT / 10\:00am PDT / 18\:00pm BST / 19\:00 CET
Speakers\:
We will randomly select one registrant for this Webinar to receive an Apple iPad. The winner will be announced during the live event.
Register now for &ldquo\;The Case for Social Media Management and Archiving&rdquo\;
The use of social media in companies has literally exploded over the past few years in virtually every organization. Yet relatively few organizations understand how it is being used\, many are taking on needless legal\, compliance\, and reputational risks\, and most IT professionals have not made the return-on-investment case internally for social media management and archiving solutions.
Join us for a special Osterman Research and Messaging News panel Webinar focused on why organizations should monitor and archive social media content and how you can justify implementing a solution in your organization.
Attendees will be able to articulate the ROI case internally for archiving and risk mitigation arguments that should be used to help quickly gain control of social media content while still experiencing its benefits. Discover\:
In short\, understand why you need to archive and manage social media\, how to make the ROI case for it internally\, and have the opportunity to ask your top social media management questions of our experts.
Register now for &ldquo\;The Case for Social Media Management and Archiving&rdquo\;
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T172159Z DTSTART;VALUE=DATE-TIME:20101027T180000Z DTEND;VALUE=DATE-TIME:20101027T200000Z UID:http://www.webinarcentral.net/content/qsr-device-inspections-%E2%80%93-transition-%E2%80%9Cbarely-surviving%E2%80%9D-%E2%80%9Cgaining-control%E2%80%9D-webinar-complianceo URL;VALUE=URI:http://www.webinarcentral.net/content/qsr-device-inspections-%E2%80%93-transition-%E2%80%9Cbarely-surviving%E2%80%9D-%E2%80%9Cgaining-control%E2%80%9D-webinar-complianceo SUMMARY:QSR Device Inspections – Transition from “Barely Surviving” to “Gaining Control” - Webinar By ComplianceOnline DESCRIPTION: \;This Medical Device Quality System training will discuss how to Create an adequate quality system that meets FDA&rsquo\;s requirements and Effectively prepare for upcoming Quality System Regulation (QSR) inspections.
\;
Areas Covered in the Seminar\:
\;
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T172159Z DTSTART;VALUE=DATE-TIME:20101027T190000Z DTEND;VALUE=DATE-TIME:20101027T190000Z UID:http://www.webinarcentral.net/content/free-webinar-generate-quality-sales-leads-using-webinars-0 URL;VALUE=URI:http://www.webinarcentral.net/content/free-webinar-generate-quality-sales-leads-using-webinars-0 SUMMARY:FREE Webinar\: Generate Quality Sales Leads Using Webinars DESCRIPTION:Generate Quality Sales Leads
~Using Webinars
Webinars are a low cost way to generate qualified sales leads. Delivered as educational marketing\, they also position you as an authority in your field\, creating respect and instilling trust in your audience. Bottom line\, it gives your sales efforts a running start.
What You Will Learn\:
• The benefits of educational marketing
• The rules of lead generation webinar engagement
• The steps to create a well organized follow-up process
• The best methods to cost-effectively attract webinar registrants
Who Should Attend\:
• Sales and Marketing professionals who know the value of their customer
• Management who wants their sales staff closing\, not cold calling
• Executives who understand long-term leadsource ROI
All Attendees will receive\: a copy of “40 FAQs About Lead Generation Webinars\\"
About the Presenter\:
Don Cameron\, Marketing Strategist and founder of Interactive Telesis and ConferTel\, has helped hundreds of organizations generate non-dues revenue by delivering educational webinars to their members in addition to helping businesses use an educational marketing approach to cost-effectively generate qualified sales leads.
Register for the webinar on Business Continuity with Virtualization and how to maximize performance while Minimizing TCO on Oct 27th 2010. Once registered you will receive an email confirming your registration with information you need to join the Webinar.
Most IT managers are continuing to look for ways to save money in the IT enterprise. One of the chief concerns for IT professionals is implementing a Business Continuity/Disaster Recovery solution. This webinar is designed to show you how to manage Business Continuity with Virtualization.
Raj Kosuri\, CTO and Terell Jones Director of Infrastructure for Ecomnets\, the industry's leading authorities on Green IT infrastructure design and management will discuss\:
• Why use virtualization as a business continuity strategy?
• How does it maximize performance?
• How does it minimize TCO?
Who Should Attend\: Professionals new to virtualization including\: CEO\, CIO\, CTO\, CFO\, CSO\, COO\, IT Managers\, Data Center Managers\, Facilities Managers\, Business Managers
About EcomNets\:
EcomNets Green IT Solutions can help you save energy costs\, save cooling costs\, and reduce your carbon footprint. EcomNets are experts in PC Power Management\, Virtualization\, Cloud Computing\, Data Center Best Practices\, and Electronic Waste Management. EcomNets can help you easily develop a Green IT strategy compatible with your business processes. EcomNets Green IT Solutions delivers fast\, flexible\, and affordable solutions\, helping you drive consistent and measurable improvements in your Green IT Initiatives.
Register for a session now by checking a date below\:
Wed\, Oct 27\, 2010 11\:00 AM - 12\:00 PM EDT
https\://www1.gotomeeting.com/register/238994081
Wed\, Dec 1\, 2010 11\:00 AM - 12\:00 PM EST
https\://www1.gotomeeting.com/register/869060065
Wed\, Jan 12\, 2011 11\:00 AM - 12\:00 PM EST
https\://www1.gotomeeting.com/register/210026305
Once registered you will receive an email confirming your registration with information you need to join the Webinar.
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