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Pharmaceutical Manufacturing Batch Record Review - Webinar by GlobalCompliancePanel

18 August 2010, Wilmington, DE, United States


Introduction
The Learning Objectives of this presentation include:

* Recognize regulatory (FDA/EU) requirements for batch records and batch record review
* Modeling best practices of a technical review of batch records
* Discover the essentials of batch record reviewer qualifications and training

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Venue
Online Training Webinar

Online Training Webinar, Wilmington, DE, 19801, United States

Useful links

Organised by
GlobalCompliancePanel
Contact information
Support
United States of America
800-447-9407
Contact us by email

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