Writing Validation Master Plans: Best Practices for Authoring a Compliant Document
Duration : 90 Minutes
Joy L. McElroy,
Joy McElroy entered the pharmaceutical industry in 1992 shortly after earning a Bachelor of Science degree at North Carolina State University. She began at Pharmacia & UpJohn performing environmental monitoring and sterility testing. From there she moved into a supervisory role at Abbott Labor Read more
This webinar will discuss the major components of a Validation Master Plans, how the VMP is different from Validation SOPs. Various regulatory requirements for Validation Master Plans. It will also highlight the effective guidelines for authoring a VMP and a team writing approach to authoring a Validation Master Plans.
Course Objectives:
Validation Master Plans discuss validation activities across an entire site or within an organization. It is a summary of validation strategies and its main purpose is to document the compliance requirements for the site and to ensure that sufficient resources are available for validation projects. Validation Master Plans may be written to cover specific departmental validation activities or the validation process for a specific type of system which assist an organization with validation strategies or provide control over a specific process.
Why Should You Attend:
This webinar will discuss the major components of Validation Master Plans. It will discuss how the VMP is different from Validation SOPs, what are the types and examples of VMPs. Various regulatory requirements for Validation Master Plans , effective guidelines for authoring a VMP and a team writing approach to authoring a Validation Master Plans will be discussed. Participants will learn how to effectively write a VMP most appropriate for their manufacturing organization.
Course Outline:
• 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
What You Get:
• Training Reference Materials
• Live Q&A with our Expert
• Participation Certificate
• Access to Signup Community (Optional)
• Reward Points
Who Will Benefit:
• Validation Engineers
• Supervisors and Managers
• Quality Assurance personnel
• Engineering Consultants
• Regulatory Personnel
• Auditors
Please reach us at 1-888-844-8963 for any further assistance or if you wish to register
