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The Online Seminar shows the Possibilities of the use of Desktop-Sharing Software. The Online-Seminar is free of charge an will contain the following topic. How to Setup the Software. The Webinar will held on request, the duration is approx. 30 Minutes Further Information to the Online-Seminar Learn more: www.practicepaysolutions.com/mastery Join us for a free series of one-hour webinars with the a team of industry experts! We're presenting the less-covered, critical issues for small business owners, so you can reduce the time you spend on set-up and administration-- and focus on what really matters. Can't attend live? We'll send you the call recordings so you can access valuable information and share the event with your community! April 2nd: The Joy of Productivity with George Kao April 16th: How to Create Profitable Referral Partnerships with Robert Notter April 24th: Say Bye-Bye to Your Boring Bio with Nancy Juetten May 15th: From Contacts to Contracts with Caterina Rando May 22nd: Red Fire Profitability with Liz Goodgold June 5th: Developing Contracts & Service Agreements with Tasha Cooper Coleman June 19th: Outsourcing Secrets with Travis Greenlee July 10th: Your Money Relationship = Your Business Success with Helen Kim July 24th: How to Play a Bigger Marketing Game with Fabienne Fredrickson Allan Gonsher and Kids Inc are pleased to a offer a series of Play Therapy Webinars. If your work with children, or want to work with children, these are workshops that you can not afford to miss. Each webinar workshop offers one hour of continuing education credit. Start: 06/14/2012 9:00 am
Course Description :- Sterilization is a critical aspect of device approval and release. Though this is indeed fact, manufacturers sterilize product as a matter of course, without expert sterilization assurance personnel to guide them through potential problems in sterilization. As the world and meaning of CAPA continue to evolve in the medical device industry, further misunderstanding arises when faced with determine root cause and corrective (or preventive) action for any variation in this critical process in device manufacture. The course will begin with an overview of EO sterilization, explaining which aspects of the process often cause confusion. This will be followed by process validation and what paperwork is required to provide ‘documented evidence’ ; and finally what are typical deficiencies encountered in the EO process. Next a detailed explanation of Radiation Sterilization will be given. Specific to Radiation Sterilization is the required sterilization dose, which will be covered in depth – how to determine sterilization dose and how to maintain the validated dose. Process validation will be covered as well as the typical deficiencies encountered in Radiation Sterilization and Validation. Critical and non-critical deficiencies will be covered and when this should trigger a CAPA. Finally contract sterilization will be reviewed with the specifics of how to deal with CAPA when you are not directly responsible for sterilization. Who will Benefit:- This course will be beneficial to the following personnel in Medical Device Manufacturing and Sterilization facilities:
Start: 06/14/2012 10:00 am
End: 06/14/2012 11:00 am
This webinar on Risk Evaluation and Mitigation Strategy (REMS) will help you understand how to adhere to REMS policy, its implementation and submission requirements. It will discuss FDA's current thinking on REMS, how it reduces the REMS obligations for sponsors, and how the agency's requirements and procedures in this area are evolving. Why Should You Attend: Risk Evaluation and Mitigation Strategy (REMS) continues to be a critical part of the FDA’s focussed efforts to increase safety of marketed products (drug or biological). As such they are enforceable by civil monetary penalties of up to $250,000 per violation that can continue to double for subsequent 30-day periods, up to $1 million per period, $10 million per proceeding. Products in violation of REMS requirements may not (continue to) be introduced into interstate commerce. Proper adherence to REMS regulations is critical. However, the implementation of a REMS can be challenging. It must be undertaken by a specified protocol, departure from which requires agreement with the FDA. This webinar will explain the above. Participants will understand when a REMS will be required, the elements that need to be included in the REMs needed for their product, as well as details of the two-part format required for submission: the proposed REMS and the more detailed REMS supporting documents. Also, the FDA requirements and procedures continue to evolve. We will adress the agency's current thinking in some instances and show how they reduce the REMS obligations for sponsors. Learning Objectives:
Start: 06/14/2012 10:00 am
End: 06/14/2012 11:30 am
This 90-minute webinar will help you understand the Americans with Disability Amendments Act (ADAA) requirements, concepts, and broad applicability of the Act. It will answer critical questions address common problems that employers face in implementing the ADAA. Why Should You Attend: Many employers think of ADAAA as an obstacle to their business. This webinar will show you how ADAA addresses some of employer concerns that the original ADA did not address, and how implementing the ADA in a way that reflects concerns of the disabled employee and the needs of employers is now easier and more realistic for the workplace. This presentation will also review an option that clients have found effective when an employee requests accommodation that is beyond the capabilities of the business to offer. This webinar will answer some of the critical questions that employers face today, and others: How can you tell if you need to offer an employee Reasonable Accommodation? What is Reasonable Accommodation? What are” Essential Duties” of a position? (Do you know it is a legal requirement of ADAAA to identify them?) Where are “Essential Duties” best recorded? What is a “Qualified Applicant with a Disability”? Why is that important? What are the penalties that a business might suffer if they are found to not have properly implemented requirements of ADAA? Who assesses the penalties? What are the chances these requirements will go away? Learning Objective: Identify ADAAA requirements, concepts, and broad applicability of the Act. Start: 06/14/2012 10:00 am
End: 06/14/2012 11:30 am
This webinar will present a methodology for system assessment, risk-analysis, 21CFR Part 11 compliance, remediation and inventory, along with templates and forms that attendees can modify for their own business. Why Should You Attend: Can you show me how you manage your computer systems in compliance with 21CFR Part 11? This presentation will describe a process which has prepared several companies to answer this question from FDA inspectors accurately, completely and to the great satisfaction of the inspectors. We will show how to inventory the site, assess the compliance risk of existing systems, implement new systems, remediate any non-compliance found, prepare SOPs and quality policies, collate the required documentation and train the staff. Attendees will learn how to prepare and present a concise and comprehensive presentation to regulatory inspectors. Preparation and knowing in advance the expectations and required deliverables for a successful inspection is critical to your pharmaceutical, medical device, biotechnology or software company. Case studies will be presented showing the outcomes for three inspections at companies following this methodology. Start: 06/14/2012 1:00 pm
End: 06/14/2012 2:00 pm
Seniors belong to a population group most affected by air pollution and indoor air contaminants – and the associated symptoms can reduce their quality of life or feeling of well-being. The best way to battle indoor air pollution is to know the facts and make informed decisions. Sign up for this free webinar offered by Air Quality Academy to find out more about • Common Indoor Air Pollutants The information in this webinar will help you take simple steps toward a cleaner and healthier indoor environment. The webinar is suitable for independent seniors and their relatives, owners/operators of retirement homes, assisted-living facilities and similar residences for seniors. (Other times and dates may be available. For more information, e-mail leif@airqualityacademy.org) About Air Quality Academy Air Quality Academy offers complimentary webinars to promote practical solutions to IAQ concerns and support preventative maintenance combined with a rational approach to avoid common air quality problems. For more information, please visit www.airqualityacademy.org Start: 06/14/2012 2:00 pm
End: 06/14/2012 3:00 pm
Indoor Air Quality is easily compromised by a variety of factors and can affect human health and well-being. Attend this webinar to find out more about Indoor Air Pollutants such as • Chemicals and VOCs The webinar will explore simple steps to improve indoor air quality in homes, buildings and small businesses, provide an overview of popular air filtration technologies and go over important considerations when it comes to air purifiers. Register now to reserve your seat for this free webinar. (Other dates and times may be available; for more information, e-mail michelle@airqualityacademy.org) About Air Quality Academy The Air Quality Academy is a free and comprehensive resource to distribute information, solutions and practical guidance related to indoor air quality concerns. Air Quality Academy offers complimentary webinars to promote practical solutions to IAQ concerns and support preventative maintenance combined with a rational approach to avoid common air quality problems. For more information, please visit www.airqualityacademy.org Start: 06/14/2012 2:30 pm
End: 06/14/2012 3:30 pm
Se servir d’Hadoop pour réaliser des traitements complexes de données (ou parfois même basiques) requiert un certain niveau technique. Pourtant, les ingénieurs ne sont pas les seuls à s’intéresser à ses capacités de traitement. Les analystes marketing, les chercheurs, les chefs de projets et autres acteurs du Big Data ont besoin d’accéder à la puissance d’Hadoop mais doivent dépendre des équipes techniques pour gérer leurs données. Ces fonctionnalités n’ont pas besoin d’être compliquées. Sans avoir à créer une seule ligne de code, nous allons vous montrer : Ce webinar aidera les passionnés du Big Data de tous niveaux à tirer profit de la puissance d’Hadoop. C’est si simple, qu’un utilisateur métier peut le faire ! Date : 14 juin 2012 de 14h30 à 15h30 Inscrivez-vous dès maintenant : https://www2.gotomeeting.com/register/532924786 Start: 06/14/2012 4:00 pm
End: 06/14/2012 5:00 pm
Free Tech Webinar Presented by Krish Ayyar, Srinivas Vippa Corp-corp provides you a new door for entering in to TOGAF World. Join with us and get the free participation Gift !!! Webinar Highlights These days, not one day passes without hearing some news or other about Social Media. It is either Facebook IPO or Instagram being taken over etc., If you take Mobile, there are millions of Apps for iPhone and Android Phones. How about Analytics? There is a lot of talk about Big Data, Hadoop etc., Also, everyone has a “Cloud” offering including Amazon, Microsoft, HP, Sales Force, IBM etc., etc. SOA the old stalwart is back in the news. SOA is being talked about in conjunction with all the other technologies mentioned here. Surely, all these trends have major impacts on the way we do business and consequently affect IT Strategy and Architecture in many organizations. Yet, we believe, the IT efforts in many organizations are at best “Knee Jerk” reactions rather than a systematic approach to address these trends. Enter TOGAF 9.1 – The latest version of The Open Group Architecture Framework. TOGAF 9.1 provides details about how SOA can be enabled within TOGAF and how to develop Enterprise and Solution Architectures. In this webinar, we will provide you with an overview of these topics. Participants also receive a PDF file of TOGAF 9.1 Quick Reference Card. Presenter’s Profile Krish is a Practitioner and Educator of Enterprise and Solution Architecture for more than 15 years. He has successfully delivered many TOGAF 9 Training Courses internationally by class room and e-learning modes since 2008 while he was with a boutique EA Consultancy and an Accredited Course Provider (ACP) of TOGAF Training. Krish complements his Training skills with practical field experience as an Enterprise Architect. He was most recently Enterprise Architect at Harvey Norman, Australia’s leading retailer where he was responsible for establishing their EA capability, Technology Plans, Standards and Enterprise. Srinivas brings a wealth of hands-on practical experience in architecting, designing and developing SOA, BPM solutions on multiple platforms. Besides being certified as SOA architect in webMethods, Oracle, Tibco, he is also TOGAF 9 certified and Project Management Professional (PMP). Registration: To register for this webinar, Visit www.corp-corp.com/blog/togaf-smacs-attack-how-do-we-architect-for-these-... There will be an opportunity to ask your questions and doubts at the end of the webinar. Register now and join with us. Feel free to forward this message to your friends and colleagues. Start: 06/14/2012 11:30 pm
Why should you Attend : By lowering the import risks to your suply chain would lead to fewer Customs inspections and delays to your freight. The reduce lead times would enhance cost savings. How to become a low risk importer eventhough you may import various commodities that have high risks like hazardous materials, products that are considered unsafe, products that do not meet CPSIA and materials coming from high risk countries. Areas Covered in the Session: Product Valuation- Tooling Royalities and Commissions Importer's Self –Assessment Security and C-TPAT Product Safety and the Customs Import Product Safety Program Intellectual Property Rights A discussion on Customs searches. Who will benefit: (Titles) Import Managers About Speaker Barry O’Brien brings extensive experience in customs, compliance, trade, import, supply chain experience, security, import product safety, trade law, global expertise, government programs, finance, budgets and trade software programs. He has experience in copyright and trademarks laws, product development and royalties’ disclosures that affect global customs compliance. At Hasbro, Barry organized the Importer’s Self-Assessment Program on trade and import product safety with the US Customs and Border Protection and he was a leader in a project to develop market opportunities in China. Barry served as the Director of Global Trade & Customs at Hasbro, Inc., where his responsibilities was to maintained the company’s low risk and high compliance rate with US Customs and Border Protection. Barry was the Chairman for the Toy Industry of America International Trade Committee, chairman of the Trade Support Network serving on the Revenue Committee and member of the Trade Support Network ITDS Committee. In October of 2004, Barry was appointed by the United States Customs and Border protection to become a Trade Ambassador. In January of 2007, the United States Department of the Treasury and the Department of Homeland Security appointed Barry to the 10th term of the Departmental Advisory Committee on Commercial Operations of Customs and Border protection (COAC). In January, 2009, the United States Department of the Treasury and the Department of Homeland Security appointed Barry to the 11th term of the Departmental Advisory Committee on Commercial Operations of Customs and Border Protection (COAC). In March of 2010 Barry accepted an award form US Customs for his contributions in working to implement, improve and strengthen the Customs-Business Partnerships in achieving trade facilitation and security of society. Barry is a speaker on the C-TPAT and ISA process for trade compliance and import product safety. Barry has addressed professional organizations, including the Coalition of New England Companies for Trade (CONECT), American Conference Institute, Marcus Evans, Council of Logistics Management and the United States Customs Trade Symposium. | ||
