Faculty: Joy McElroy


  • Date: 10/13/2022 11:00 AM - 10/13/2022 12:30 PM
  • Location: Online Event

Tickets


Ticket Type
Qty
Live- Single
$200.00
0
For ONE Participant – Live session only
Live Corporate
$700.00
0
For Maximum of 10 participants – Live session only
Recording - Single
$350.00
0
Recording access for ONE participant (viewer) – Unlimited viewing access for 6 months
Recording - Corporate
$1400.00
0
Recording access (Multiple licenses) for up to 10 participants – Unlimited viewing access for 6 months

Total

$0.00

Description

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