Description :Every medical device company (OEM) must meet certain standards for validation of its transfer plans, facilities, clean rooms and processes. These standards apply for OEM’s and suppliers to OEM’s. Many medical companies have never had a Master Validation Plan for their facilities, processes or suppliers. This is an important standard to have when being audited to show on big picture compliance to FDA and foreign standards.This webinar on “How to Develop a Master Validation Plan” (also known as Validation Master Plan) will provide a step-by-step procedure for all medical device companies and their suppliers that are in need of developing a plan for product/equipment transfer, facilities, processes or to develop a company standard.Areas Covered in the Session :Master Validation Plan contentRevision historyBackgroundObjectivePurposeScopeProject approachKey activitiesProject organizationCommunication planQuality AssuranceFacility approachValidation approachScheduleBudget ...and moreWho Will Benefit:OEM Senior managementSupplier Senior managementManagers and directorsManagers setting up new facilities and product linesPlant and facility managersEnd-users responsible for design control and product developmentR&D and product developmentProject managersFacility and clean room designersProcess engineers and managersValidation engineersQuality management and engineersAuditorsSuppliers to medical OEM’sConsultants