Compliance Trainings, Online
2015-06-12
Description : This course will provide a step-by-step guidance for medical device companies that need to develop a validation master plan (VMP) for product/equipment transfer, facilities, processes or to develop a company standard. This course will provide guidance on best practices for developing and implementing a good plan detailing responsibilities, and deliverables to make validation efficient, and consistent. The Validation Master Plan describes the way an organization approaches validation; who controls the various aspects of the validation activities; and how production, quality, and management will be involved. The VMP also details the validation requirements for each test/ system/ equipment and will guide the organization in achieving its objectives. Areas Covered in the Session : What is a VMP and how is it valuable to my company? What topics are covered in the VMP and to what extent? How is the VMP controlled and updated? How is the VMP implemented? Who contributes to the VMP? Overview of Validation Master Plan What is a VMP? Which regulations apply? What topics are covered in the VMP? Master Validation Plan content Purpose Scope Project approach Key activities Project organization Communication plan Quality assurance Who are the VMP Key contributors? Defining their roles Quality Assurance Regulatory Affairs Operations Engineering Implementation of the VMP Training requirements Controlling and updating the VMP Who Will Benefit: Quality Assurance Teams Regulatory affairs Teams Operations Teams Engineers Teams Quality Engineers Teams Price tags: Live Single Live : For One Participant $ 249 Corporate Live : For Max. 10 Participants $ 899 Recording Single REC : For One Participant - Unlimited Access for 6 Months $ 299 For more information and enquiries contact us at Compliance Trainings 5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada
Customer Support : #416-915-4458
Email : support@compliancetrainings.com
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