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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 EURUSDGBP

Aquaporins, Vol 51. Current Topics in Membranes

Aquaporins summarizes the present knowledge in this expanding field of research, starting with the structural analysis of water channel proteins. Subsequent chapters begin with mammalian aquaporins,...

Published:  April 2001
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