Develop, Execute and Enforce an Effective Validation Master Plan - June 17 , 2008
The VMP is a document that has never been mandatory, but can be one of the first documents a regulator will ask to view but most companies are using them. This webinar will provide valuable assistance and guidance to all life sciences manufacturers that are preparing to use or are currently using validation master plans to bullet-proof their validation programs.
Risk-Based Software V&V - FDA,GAMP, 14971 - June 17, 2008
this webinar will explain how to employ equipment / process DQs, IQs, OQs, and PQs, against a background of limited company resources
Implementing a GCP Vendor Qualification Program: Ensuring your vendors are in compliance with FDA requirements June 19, 2008
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