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

Combination Products - The FDA's New Codification of the cGMP Requirements Applicable to Combination Products - 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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An Introduction to Good Manufacturing Practice for Medicinal Products - E-Learning Module

Good Manufacturing Practice (GMP) is a set of rules for medicines manufacturers to follow so that their products are safe, effective, and of good quality. The rules may be written into law or set out...

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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) - 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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Vaccine Contract Manufacturing Market, 2016 - 2026

The "Vaccine Contract Manufacturing Market, 2016 – 2026" report provides an extensive study of the current market landscape of CMOs focused on vaccines. The study presents an in-depth analysis of a...

Published:  June 2016
Price:  From
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