Webinars
Event
- Title:
- PAI Audits: Are You Ready?
- When:
- 10.28.2010
- Category:
- Quality Assurance & Auditing
Description
Webinar Date: October 28, 2010 Time: 11:00 to 11:30 PST
Summary: The FDA's Pre-approval Inspection process is a critical time-to-market prerequisite to getting your product licensed and approved for commercial manufacturing.
Join us on Thursday, October 28, 2010 at 11:00 PST to to gain insight on best practices for:
- Increasing your probability of success in passing your FDA PAI
- Clearly demonstrating that your manufacturing establishment or contract manufacturing organization has the capability to manufacture your product
- Maximizing your contribution to the FDA's assurance that submitted data in your NDA, ANDA or BLA are accurate and complete
Sponsored By: USDM's Quality Assurance & Auditing Practice Learn More
Visit our website to register for additional Quality Assurance & Auditing Webinars
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Recorded Webinars
About USDM
USDM is a leading global consulting firm focused on life sciences. We specialize in regulated business processes, with an emphasis on compliance and performance.
USDM provides innovative services and solutions that enable life science companies to achieve and maintain compliance across the entire enterprise.
