Production and Process Controls for Medical Device Companies
May 6, 2020 - CA USCompliance4all
support@compliance4All.com
Phone:8004479407
Overview:Production and Process Controls (P&PC) are one of the key capabilities necessary for medical device companies to consistently and effectively produce safe and effective products.Because Production and Process Controls are so critical they are one of the major subsystems emphasized in inspections by the FDA.Why you should Attend: Failure to adequately implement Production and Process Controls (P&PC) can lead to disaster for your company or even worse for your customer. And P&PC continues to be a leading cause of 483 and warning letter observations from the FDA.Even more alarming, P&PC failures are a leading cause for complaints, malfunctions, and product recalls. This webinar can help you prevent serious issues such as these.You'll learn about FDA quality system regulation expectations, and how you can successfully and efficiently establish these into your Quality Management System. Join us to learn the essentials of Production and Process Controls.Areas Covered in the Session:Establishing P&PCChange ControlEnvironmental ControlPersonnel RequirementsContamination ControlBuildingsEquipmentManufacturing MaterialAutomated ProcessesInspection, Measuring, and Test EquipmentProcess ValidationLinkages to the total product life cycle and risk managementProcess ImprovementLearning Objectives:Overview of the RegulationsFDA ExpectationsLessons Learned and Common MistakesBest PracticesPreparing for an FDA InspectionWho Will Benefit:AuditorsQuality EngineersManufacturing EngineersEngineering ManagersManufacturing SupervisorsManufacturing/ Production /Operations Supervisors, Managers, and DirectorsPlant ManagersQuality ManagersEmployees new to Medical Device CompaniesSpeaker ProfileSusanne 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. While at GE, J&J, and Medtronic, Susanne worked in various world-wide roles including Executive Business Consultant, WW Director of Quality Engineering and, Design Quality, and Director of Corporate Compliance. 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.Event link:https://www.compliance4all.com/webinar/--502945LIVE?channel=clinicalleader-May_2020_SEOContact InfoNetzealous LLC, DBA -Compliance4allEmail: support@compliance4All.comPhone: +1-800-447-9407Website: https://www.compliance4all.com/