This webinar will discuss the major components of Validation Master Plans. It will discuss how the VMP is different from Validation SOPs. Various regulatory requirements for Validation Master Plans will be discussed as well as effective guidelines for authoring a VMP and a team writing approach to authoring a Validation Master Plans will be discussed.
Various types and examples of VMPs will be given and discussed. Participants will learn how to effectively write a VMP most appropriate for their manufacturing organization. Why should you Attend: Attendees should register to learn the major components of a Validation Master Plans. They will learn how the VMP is different from Validation SOPs.
Areas Covered in the Session :
What is a VMP and what is its intended use
How is a VMP different that validation SOPs
Components of a VMP
Regulatory requirements for a VMP
Team Writing a VMP
Examples of VMPs
Effective writing practices for an audit-ready document
Who Should Attend:
Quality Assurance Departments
Quality Control Departments
Research and Development Departments
Regulatory Affairs Departments
Engineering Departments
Validation Departments
Documentation Departments
Consultants
Auditors