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Start: 07/20/2010 8:00 am
End: 07/20/2010 9:00 am
This CAPA training will helps in methodologies of Six Sigma and CAPA converging and how to recognize which methodology is best to use for a problem.
Why Should You Attend:
Simply documenting "it broke - I fixed it" does very little to instill permanent solutions. Six Sigma methodologies is an ideal toolbox for drilling into the root causes of problems and making certain that permanent solutions are in place. The true spirit of CAPA and Six Sigma is the improvement for the overall system and the reduction in variation around a previously established "centered" process. Too many companies focus on the speed with which CAPAs are closed, yet pay too little attention to the effectiveness and longevity of the solution.
Competing Six Sigma and CAPA processes are creating duplication and drawing from same resources. Projects have to be documented in two ways – one for CAPA and another for Six Sigma. Attend this Webinar to Lean how to integrate both so the organization gets the best of both worlds – CAPA and Six Sigma.
Areas Covered in the Seminar:
- Why are the methodologies of Six Sigma and CAPA converging?
- Why do companies have duplicate and competing Six Sigma and CAPA programs.
- How to recognize which methodology is best to use for a problem.
- How should my quality systems work together?
- Best Practices.
- Should Electronic Signatures apply to my Enterprise Six Sigma system?
Note: Use this Promo Code(100759) to avail Discount of 10% on LIVE Purchase.
Start: 07/20/2010 9:00 am
End: 07/20/2010 10:15 am
Learn FDA requirements for 21 CFR Part 11, understand how to implement with the help of SOPs and case studies.
Why Should You Attend:
Though FDA's new Part 11 regulation takes quite some time, but inspectors go out and inspect computer systems and e-records for compliance with GMPs and most recent Part11 interpretations. Just in 2007/2010, there have been about 30 Warning Letters related to Part 11 compliance, some with disastrous consequences for inspected companies. It seems that 'enforcement discretion' as stated in the 2003 guidance is not applied any more. Also FDA's computer expert John Murray recommended at a conference to follow 21 CFR Part 820 also for drug companies. This seminar will give a good understanding of current and future FDA requirements for 21 CFR Part 11 and provide steps, examples and tools for cost-effective implementation. Attendees will receive SOP to define and document scope and control of part 11. Along with it 15 case studies containing step by step description and recommendation for part 11 requirements.
Areas Covered in the Seminar :
- FDA's current inspection and enforcement practices.
- FDA's current interpretation: learning from FDA guidance, and FDA conference presentations and discussions.
- Learning from FDA inspection reports.
- Part 11 and the new EU Annex 11: similarity and differences.
- Strategy for cost-effective implementation of the 'new' Part 11:A six step plan.
- Recommended changes to existing Part 11 programs to reduce costs.
- Justification and documentation for the FDA and your management.
- Going through case studies from laboratories, offices and manufacturing.
- Preparing for Part 11 Inspections.
Start: 07/20/2010 11:00 am
How Can Your Organization Build a Scientific Roadmap to World Class Performance on the Key Business Outcomes?
Organizations lack science in managing, measuring and improving business processes. Attend this webinar to gain insight from Genpact’s OTC Practice Leader Mark Wood into how to achieve an end-to-end process view, and focus on improving effectiveness metrics rather than efficiency metrics. Learn how to measure some critical business outcomes, such as Revenue Dilution, as the opportunity gain is 5 to 10 times the impact achieved through reducing costs.
Join this webinar to find out how Genpact’s Order To Cash SEP can help you maximize business impact for your company. Key learnings from this session include:
A granular approach to process management and measurement
Critical business outcomes for the Order to Cash process including a deep dive into Revenue Dilution
Top performance measures and drivers and the linkages to business outcomes
Key process and technology Insights that significantly impact your business outcomes
Start: 07/20/2010 11:00 am
End: 07/20/2010 11:00 am
Master Data Management provides a consistent and reliable source of truth for any critical data assets such as suppliers, locations, employees, customers, contracts, projects and even cross system reference data.
Gaining alignment of your important data, helps you gain alignment across your organization and ultimately save dollars along the way.
During this webinar on MDM/governance opportunities and pitfalls, you will learn:
•How to build a business case for MDM and governance
•The top THREE reasons for failed MDM business cases and how to avoid them
•How to find opportunities to start small with MDM
•The FIVE steps to a successful master data management project
•Essential resources and the tools you need for success
Download Talend MDM Community Edition today: http://www.talend.com/download_form.php?cont=mdm
Consulting and implementation partner Decision Technologies: www.DecisionTechnologies.com
Register Today : http://nxy.in/zw2ml
Tue, Jul 20, 2010 11:00 AM - 12:00 PM PDT
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Start: 07/21/2010 10:00 am
End: 07/21/2010 11:00 am
This FDA Software Validation and Verification training/webinar will review the validation planning process with particular emphasis on avoiding six common pitfalls.
Why should you Attend
- FDA inspectors are now being trained to evaluate software validation practices.
- Increasing use of automated manufacturing and quality systems means increased exposure.
- Most recalls can be traced back to computerized equipment, exposing the validation process to scrutiny.
- Corporate uncertainty leads to inaction and 'wheel spinning'.
- A third of recent warning letters included citations with respect to improper or ineffective validation.
Many companies struggle with understanding how to avoid major mistakes when validating software to FDA standards. This presentation will review the validation planning process with particular emphasis on avoiding six common pitfalls. The attendee should leave the presentation confident in their ability to improve the level of validation success.
Areas Covered in the seminar:
- Outline of FDA regulations as applied to software.
- Review of FDA software validation requirements.
- Why validation makes good business sense.
- The 6 Most Common Problems in FDA Software Validation & Verification.
- Strategies on how to avoid the most common problems.
- Advice on successful validation project staffing.
Note: Use this Promo Code(100759) to avail Discount of 10% on LIVE Purchase.
Start: 07/21/2010 2:00 pm
End: 07/21/2010 3:00 pm
Psst...think workplace gossip is harmless? Think again.
Gossip can torpedo employee morale, destroy working relationships, and foster a climate of distrust. Gossip results in decreased productivity, leads to attrition, and may ultimately expose your company to liability. In this one-hour webinar, we will explore several practical ways to neutralize gossip both from a managerial perspective and on an individual level. Discover how to effectively respond to someone who approaches you with gossip and what steps to take if you ever find yourself the subject of gossip in your office.
The registration fee is $35. For your convenience, you can register and make your payment online at http://www.marigoldconsulting.com/Registration.
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Start: 07/22/2010 10:00 am
End: 07/22/2010 11:00 am
Attend this Webinar to understand how to implement/change a dress code policy or how to make process so as to spend less time on dress-code-related problems.
Why Should You Attend:
- Can you require an employee to hide her tattoos?
- Can you legally require an employee to take out their tongue ring during work hours?
- Does a dress code mandating facial hair and other grooming policies invite a race discrimination claim?
- Can an employee legitimately dispute a no-smoking policy?
Today, plaintiffs are using traditional discrimination concepts to push the envelope in making claims of lifestyle discrimination based upon sexual orientation, gender-identity, physical appearance, pornography, piercings, tattoos, smoking and other borderline privacy/personal issues.
Areas Covered in the Seminar:
- How to Change Your Company Dress Code (or institute one) Without Causing a Revolt.
- Exactly What to Say to a Smelly Employee.
- How to Handle Provocative Clothing (and what word not to use).
- Where Dress Codes and Discrimination Claims Meet (and how to avoid them).
- How Far You Can Go in Prohibiting Offensive Slogans on Workers’ Clothes.
- How to Deal with Transgender Dress-Related Issues.
- Where the Legal Line is Drawn When You Have Separate Dress Codes for Men and Women.
- How to Tailor Your Dress Code to Fit Workers in Different Types of Jobs-- From the Warehouse to the Corner Office.
- Details You Should Include in Your Written Appearance Policies.
- How to Effectively Communicate Your Dress Code Expectations to Workers.
- Dealing with Employees Who Consistently Push the Dress Code Envelope.
Note: Use this Promo Code(100861) to avail Discount of 10% on LIVE Purchase.
Start: 07/22/2010 10:00 am
End: 07/22/2010 11:00 am
This CAPA investigation training webinar will discuss FDA’s techniques to do CAPA inspection, what the FDA tells their inspectors to focus in the QSIT document and how your company can use the QSIT document to prepare for inspection.
Description:
This session will discuss what the FDA tells their inspectors, and how they train them, including a detailed analysis of the CAPA training.What should I expect the FDA investigator to look at when they visit? The FDA inspection can be much easier to handle and manage if you know what to expect. Advance knowledge will enable you to prepare for the FDA inspection. This knowledge and planning will make the inspection experience much less stressful, and assure better compliance. This session will discuss what the FDA tells their inspectors, and how they train them, including a detailed analysis of the CAPA training. Also contained in this session will be a section-by-section summary of the QSIT, the document by which FDA inspectors operate during an inspection, as well as how your company can use that same document in your preparation.
Areas Covered in the seminar:
- How to prepare for an FDA inspection?
- Development and contents of an SOP for FDA inspection.
- Reliance of FDA inspectors on compliance program guide manuals.
- Reliance of FDA inspectors on other external sources.
- Personnel training before inspection.
- In depth review and summary of QSIT.
- Use of QSIT for internal auditing.
Note: Use this Promo Code(100861) to avail Discount of 10% on LIVE Purchase.
Start: 07/22/2010 11:00 am
End: 07/22/2010 11:00 am
Complimentary Webinar - How to Promote your Business using Facebook.
This is the next generation of Facebook and the Internet - find out where you need to be and if your business is ready for the future of lead generation using Social Networks.
In working with hundreds of companies to find new business, Dean DeLisle has assembled the top items that their clients are using to generate new business in Facebook. Dean will show you how companies are using the newest features of Facebook to reach new customers and retain the ones they have.
He will also cover ways to leverage Facebook to help enhance your Search Engine Optimization!
You will Learn How to:
-Use a Facebook Page to get New Leads
-Leverage Facebook for Customer Service
-Drive Prospects from Outside Facebook to Your Business
-Setup New Facebook Advertising
*If you cannot make the specified time, by registering, you will receive access to the recording.
We look forward to seeing you in class!
“Thanks to Dean DeLisle and his guidance on Social Networks, we are seeing consistent growth and a wider reach than we could ever afford with traditional advertising. The classes and coaching have saved us thousands!” – Mark F. – CenterCars.com
ALL CLASSES ARE TAKEN ONLINE USING THE CONVENIENCE OF YOUR COMPUTER - LIVE AND RECORDED!
all day
Time: 14:15 GMT
Join international business & HR guru Lynda Gratton, Professor of Management Practice at London Business School for our webinar as she unveils the findings from the first phase of her ground breaking global research project on The Future of Work.
Lynda will be calling on this webinar’s audience to drive the second phase of the research. This is your chance to join the panel of over 200 senior executives from leading global corporations and share your thoughts on the way we will be working in 2020. The culmination of the research project is to provide you with action-oriented tools to future-proof your business and support a radically different way of working.
Webinar: Understanding the forces that shape the way we work – Preparing for the future
Organisations today face some of the greatest challenges in the history of business as social, political, and trading conditions rapidly change. The key drivers are:
• recessionary environment
• ageing workforce
• worker mobility vs a low carbon society
• globalization
• rapid pace of technological development
This webinar will answer the following questions:
• How do organisations support the development of a ‘future proofed’ leadership pool?
• How will we work when five billion people are connected all the time?
• What will be the meaning of free computing power in the business environment?
How will we work when the world population moves to cities?
• What will be the impact of oil price rise and carbon tax on the way we work?
• How do we create optimum team structures when the world is going virtual?
• What business models will be prevalent?
• What will the role of HR be in the Future of Work?
This event is selling out fast due to the limited number of places. Book now to be a part of it: http://www.wtgwebinar.com/webinar/the-future-of-work/115
Technical Requirements
- PC headset
- PC speakers
- Broadband Connection
Start: 07/22/2010 2:15 pm
End: 07/22/2010 3:15 pm
Join international business & HR guru Lynda Gratton, Professor of Management Practice at London Business School for our webinar as she unveils the findings from the first phase of her ground breaking global research project on The Future of Work.
Lynda will be calling on this webinars audience to drive the second phase of the research. This is your chance to join the panel of over 200 senior executives from leading global corporations and share your thoughts on the way we will be working in 2020. The culmination of the research project is to provide you with action-oriented tools to future-proof your business and support a radically different way of working.
Webinar: Understanding the forces that shape the way we work – Preparing for the future
Organisations today face some of the greatest challenges in the history of business as social, political, and trading conditions rapidly change. The key drivers are:
• recessionary environment
• ageing workforce
• worker mobility v a low carbon society
• globalization
• rapid pace of technological development
This webinar will answer the following questions:
• How do organisations support the development of a ‘future proofed’ leadership pool?
• How will we work when five billion people are connected all the time?
• What will be the meaning of free computing power in the business environment?
How will we work when the world population moves to cities?
• What will be the impact of oil price rise and carbon tax on the way we work?
• How do we create optimum team structures when the world is going virtual?
• What business models will be prevalent?
• What will the role of HR be in the Future of Work?
This event will sell out. Book now to be a part of it:
http://www.wtgwebinar.com/webinar/the-future-of-work/115
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Start: 07/23/2010 10:00 am
End: 07/23/2010 11:00 am
Why Should You Attend:
Health related quality of life (HRQOL) research is designed to measure patients’ input into the effects of disease and/or treatment and possibly to distinguish between treatments or devices; however it is fundamentally different than traditional medical assessments. HRQOL is not efficacy or safety, yet it can provide an alternative and valuable medical insight.
This webinar presents an introduction to HRQOL that will crystallize knowledge of underlying concepts, strategies, and processes; it will facilitate the attendees’ ability to be conversant, to assist in planning studies, and to avoid common mistakes. Additionally, it is designed to allow for accurate interpretation of HRQOL results and increase the probability of research success. Also, the FDA regulatory implications for PROs will be discussed.
Areas Covered in the Seminar:
- Defining health-related quality of life (HRQOL).
- FDA Guidance.
- Labeling/Package Insert Issues: US and EU.
- Why do HRQOL research?.
- Generic vs disease-specific instruments.
- Examples of questions and questionnaires.
- Scoring questionnaires.
- Psychometric properties - reliability/reproducibility, validity, and responsiveness.
- When to do HRQOL in the drug development process.
- Monitoring issues.
- Statistical issues.
- Proper placement in the protocol and study report.
- References/Bibliography.
Note: Use this Promo Code(101197) to avail Discount of 10% on LIVE Purchase.
Start: 07/23/2010 11:00 am
The ABCs of Webinars
~Learn the Basics from Promotion to Delivery
Webinars have become a universal method for delivering education & training programs as well as generating sales leads - and you need to know how they work and what is involved in making them a success.
What You Will Learn:
• Each step in the delivery process – Identify all of the required elements needed from start to finish to produce professional webinars.
• Tips to dramatically improve attendance – Learn how to attract the right type of participant, create compelling marketing materials and maximize promotion budgets.
• The key to generating revenue with no up-front costs or risk – Discover the easiest way to increase income without making a huge financial investment.
What You Will Get:
• A FREE webinar planning timeline
• 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.
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