Webinar Date:  March 2, 2010     Time: 12:00 to 12:30 PST

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A Validation Master Plan is a crucial document that is created at the outset of a new facility or existing facility expansion. It drives the entire validation effort and ensures the various vendors involved in the expansion align with a single validation approach.

Are you interested in what should be covered in a validation master plan?

Then join our discussion on Tuesday, March 2,  2010 where a case study that outlines the validation master plan for a sterile manufacturing facility will be discussed. The discussion will include:

• How to scope out the validation effort?
• How to set up project controls?
• Establishing a CSV and Equipment validation strategy
• Establishing Cleaning Validation, Process Validation and Media Fill strategies
• Establishing approaches for Environmental Monitoring
• Establishing approaches for Process Filtration
• Establishing approaches for Finished Product Testing
• Establishing approaches for Personnel Training and Management
• Standardizing on vendor documentation with Turn Over
  Templates

Discover and discuss this topic with the USDM experts and your peers in the industry!

Sponsored By: USDM's Manufacturing Practice  Learn More

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