WEBINAR TRAINING ON POST MARKET SURVEILLANCE OF ME 2017 - Spotlight on Post Market Surveillance -By AtoZ Compliance
Website http://www.atozcompliance.com/trainings-webinar/life-sciences/medical-devices/post-market-surveillan |
Category Medical Device;Healthcare;Quality Control
Deadline: February 09, 2017 | Date: February 09, 2017
Venue/Country: Online, U.S.A
Updated: 2017-01-09 19:10:36 (GMT+9)
Call For Papers - CFPKey Take Away :This webinar will discuss the essentials of Post Market Surveillance, how you can develop your capabilities and how PMS can provide you with important information to improve your device, better service your customers, and reduce the risk of adverse events.Overview :Post Market Surveillance (PMS) is the practice and system of monitoring the safety awareness training of a medical device after it has been released on the market. It relies on several foundations including unique device identifiers (UDI), electronic health records and medical device reporting, device registries, and advance methods for evidence generation, data analysis and vigilance awareness training. It is a system that continues to develop and improve.Why Should You Attend :Post Market Surveillance is an essential part of the FDA’s mandate to protect the public health. This Post Market Surveillance and Vigilance Webinar will establish why it is something that every medical device company needs to understand to ensure product safety and effectiveness and customer satisfaction.Areas Covered In This Webinar :Overview and DefinitionsFDA Expectations, RegulationsLessons Learned and Enforcement Case StudiesMedical Device ReportingLearning Objectives :Investigating a complaint or MDRFAERS – FDA Adverse Event Reporting SystemCommon Mistakes and how to avoid themBest PracticesPreparing for an FDA or NB InspectionWho Will Benefit :Complaint Specialists and ManagersIndividuals participating in Failure InvestigationsIndividuals analyzing Returned Products/Complaint AnalysisRegulatory Affairs PersonnelQuality EngineersClinical Affairs PersonnelComplaint Handling Unit PersonnelCompliance SpecialistsFor more information, please visit : http://www.atozcompliance.com/trainings-webinar/life-sciences/medical-devices/post-market-surveillance-and-vigilance-webinar-training/susanne-manz/300201Email: firstname.lastname@example.org Toll Free: +1- 844-414-1400Tel: +1-516-900-5509Level: IntermediateSpeakers Profile :Susanne ManzSusanne Manz, MBA, MBB, RAC, CQA is an accomplished leader in the medical device industry with emphasis on quality, compliance, and six sigma. She has an extensive background in quality and compliance for medical devices from new product development, to operations, to post-market activities. Susanne has a BS in Biomedical Engineering and an MBA from the University of NM. She earned her Black Belt and Master Black Belt certifications while at Johnson and Johnson. Susanne also holds Regulatory Affairs Certification (RAC) from RAPS and Certified Quality Auditor (CQA) certification from the American Society for Quality. Susanne has now established a consulting business with a mission to provide services to help medical device companies achieve world-class quality and compliance.
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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