Writing Validation Master Plans: Best Practices for Authoring a Compliant Document
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.Validation Master Plans discuss validation activities across an entire site or within an organization. The Validation Master Plan is a summary of validation strategies. The purpose of Validation Master Plans 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. Validation Master plans are written to assist an organization with validation strategies or to provide control over a specific process.Areas Covered What is a VMP and what is its intended useHow is a VMP different that validation SOPsComponents of a VMPRegulatory requirements for a VMPTeam Writing a VMPExamples of VMPsEffective writing practices for an audit-ready documentWho Should Attend Validation EngineersSupervisors and ManagersQuality Assurance personnelEngineering ConsultantsRegulatory PersonnelAuditorsWhy 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. 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.
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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.
Validation Master Plans discuss validation activities across an entire site or within an organization. The Validation Master Plan is a summary of validation strategies. The purpose of Validation Master Plans 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. Validation Master plans are written to assist an organization with validation strategies or to provide control over a specific process.
Areas Covered
- 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
- Validation Engineers
- Supervisors and Managers
- Quality Assurance personnel
- Engineering Consultants
- Regulatory Personnel
- Auditors
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. 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.
