Usa 2016 webinar by Compliance4all on Product Risk Management Under ISO 14971
Overview: The U.S. FDA has stated that the use of a medical device or pharmaceuticals entails some degree of risk. In fact, any medical procedure / intervention does. A manufacturer is responsible to identify those risks, and take reasonable steps to mitigate them as far as practical and given the 'state of the art' at the time. ISO 14971 and ICH Q9 provide accepted methodologies by which to perform and document such an analysis and is accepted by the FDA. Areas Covered in the Session: The Revised ISO 14971:2007 for Devices ICH Q9 for Pharma Product Hazard Analysis Design, Process, and Use[r] Failure Mode, Effects and Criticality Analysis Fault Tree Analysis The Team and Its Involvement Who, When and How Product Risk Management File and Report Using the Completed Document Its Real Value Keeping it "In the Loop" Who Will Benefit: Senior Management, Project Leaders Internal / External Auditors and/or Consultants Regulatory Affairs Quality Systems Personnel / QAE New product development, Marketing and R&D Product and Process / Manufacturing Engineering Staff Document Control Speaker Profile: John E Lincoln is a medical device and regulatory affairs consultant. He has helped companies to implement or modify their GMP systems and procedures, product risk management, U.S. FDA responses. In addition, he has successfully designed, written and run all types of process, equipment and software qualifications/validations, which have passed FDA audit or submission scrutiny, and described in peer-reviewed technical articles, and workshops, world wide. Contact Detail: Compliance4All DBA NetZealous, Phone: +1-800-447-9407 Email: support@compliance4All.com http://www.compliance4all.com/ Event Link : http://www.compliance4all.com/control/w_product/~product_id=500822LIVE? Twitter Follow us https://twitter.com/compliance4all Facebook Like us https://www.facebook.com/Compliance4all LinkedIn Like us https://www.linkedin.com/company/compliance4all
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