Essentials of Complaint Handling and Medical Device Reporting
Website https://goo.gl/N1irBj |
Category fda approval for medical devices, medical device risk management, medical device recalls, fda medical device regulations, medical device training, fda regulations for medical devices
Deadline: April 20, 2017 | Date: April 20, 2017
Venue/Country: New Hyde Park, U.S.A
Updated: 2017-03-06 19:32:05 (GMT+9)
Call For Papers - CFPOverview:Complaint management and Medical Device Reporting (MDR) are critical quality systems for you to meet the needs of your 3 key stakeholders – the customer, the regulators, and your business. This medical device training will help you to understand the expectations of complaint handling and medical device reporting. You’ll learn about FDA expectations and regulations as well as lessons learned from 483s and warning letters. We’ll discuss how you can develop your processes to efficiently and effectively manage complaints and MDRs. In addition, we’ll discuss how to link these processes to failure investigation, recalls, and CAPA (Corrective and Preventive Action). We’ll cover best practices so you can be prepared for an FDA inspection.Why Should You Attend:Complaint Handling and Medical Device Reporting are considered critical processes by the FDA in maintaining the public safety. Because they are so critical they are frequently inspected areas by the FDA. More importantly, complaints can also be an early warning of issues with your products and customer problems.Areas Covered in this Webinar:Overview and DefinitionsFDA Expectations, RegulationsLessons Learned and Enforcement Case StudiesProcesses and ProceduresReportability CriteriaInvestigating a complaint or MDRLinkages between Complaint Handling, MDRs, and CAPACommon Mistakes and how to avoid themBest PracticesPreparing for an FDA or NB InspectionLearning Objectives:The objective of this webinar is to have an efficient and effective process for managing, analyzing, trending, and reporting product problems. This session will also cover the basics of complaint management, regulatory requirements for medical devices and medical device reporting.Who Will Benefit:Complaint Specialists and ManagersIndividuals participating in Failure InvestigationsIndividuals analyzing returned products / Complaint AnalysisRegulatory AffairsQuality EngineersClinical AffairsComplaint Handling Unit PersonnelCompliance SpecialistsSpeaker Profile:Susanne 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.
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