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Search for: "Quality Assurance Compliance. Procedures for Pharmaceutical and Biotechnology Manufacturers"

Supplier Qualification in the Pharmaceutical Supply Chain ( ON My Call) - Webinar

The importance of supplier qualification in the pharmaceutical supply chain continues to be a growing concern for global regulatory authorities. Over the past decade, there have been many instances...

Published:  May 2016
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Combination Products - The FDA's New Codification of the cGMP Requirements Applicable to Combination Products - Recorded Webinar

The FDA has ensured that clear FDA requirements were in place for drugs, devices, biological produces as well as Human Cells, Tissues and Cellular and Tissue-Based Products (HCT/Ps). However, there...

Published:  January 2016
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Quality Metrics and Risk Based Inspections; FDA's New July 2015 "Request for Quality Metrics Guidance for Industry" & Safety and Innovation Act (FDASIA) - Recorded Webinar

The FDA Safety and Innovation Act (FDASIA) of 2012 provides a firm legal basis for setting clearer standards for collecting data to assess manufacturing operations. Section 705 of FDASIA requires FDA...

Published:  October 2015
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Executive Report on Strategies in Barbados

How to Strategically Evaluate Barbados Perhaps the most efficient way of evaluating Barbados is to consider key dimensions which themselves are composites of multiple factors. Composite portfolio...

Published:  June 2007
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