Post Market Surveillance For Medical Devices Webinar By Globalcompliancepanel

May 15, 18 Post Market Surveillance For Medical Devices Webinar By Globalcompliancepanel

Post Market Surveillance For Medical Devices Webinar By Globalcompliancepanel

New regulations are emerging in the countries where in fact the devices manufacturers marketplace their products. The pure level of rules and rules can be daunting, however the variations in each geographic marketplace can be frightening. This webinar clarifies the areas of post marketplace surveillance that will assist you understand and put into action them.

The webinar explains the usage of post-market surveillance in keeping your risk administration file (ISO 14971) and updating your clinical evaluation (MDD Annex X). Furthermore, the webinar compares and comparison the guidelines for adverse event reporting in america, EU, and Canada.

Why you need to attend: Post marketplace surveillance could be complicated, but by breaking it into its parts, it could be accessible. With the knowledge of the parts, you can form and implement a thorough system that will assist you stay static in compliance. By going to this webinar, you will discover what you have to do and become well on the path to effective performance.

Areas Covered In the Program:The Framework of Post Marketplace SurveillanceUS SystemComplaints (QSR)Medical Gadget ReportsCorrections and RemovalsInternational SystemsComplaints (ISO 13485)EU VigilanceEU FSCA and FSNCanada Adverse Event ReportingPost Creation Information CollectionRisk Administration (ISO 14971)Clinical Evaluation (MDD Annex X)

Who’ll benefit:Quality ManagersRegulatory Affairs ManagersRisk ManagersDesign Control Managers

Dan may be the President of Ombu Enterprises, LLC, a company giving teaching and execution in Operational Excellence, centered on analytic abilities and a systems method of operations administration. Dan has a lot more than 30 years encounter in quality, procedures, and program administration in regulated sectors including aviation, protection, medical devices, and medical labs. He includes a Masters Level in Mathematics; can be an ASQ qualified Biomedical Auditor, Quality Auditor, Quality Engineer, Dependability Engineer, and Six Sigma Dark Belt; and is qualified by APICS in Source Management.

Thursday, March 22, 201210:00 AM PST 01:00 PM EST

Price List:Live : $245.00Corporate live : $995.00Documented : $295.00

webinars@globalcompliancepanel.com

Phone: 800-447-9407Fax: 302-288-6884

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