Webinar On How to Develop a Master Validation Plan
January 27, 2015 - Mississauga ON CACompliance Trainings
uttam@compliancetrainings.com
Phone:4169154458
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 content Revision history Background Objective Purpose Scope Project approach Key activities Project organization Communication plan Quality Assurance Facility approach Validation approach Schedule Budget ...and more Who Will Benefit: OEM Senior management Supplier Senior management Managers and directors Managers setting up new facilities and product lines Plant and facility managers End-users responsible for design control and product development R&D and product development Project managers Facility and clean room designers Process engineers and managers Validation engineers Quality management and engineers Auditors Suppliers to medical OEM’s Consultants