Sweet Deception: Why Splenda, NutraSweet, and the FDA May Be Hazardous to Your Health [Audiobook] English | ASIN: B0BTJXWDNJ | 2023 | 9 hours and 3 minutes | M4B@64 kbps | 259 MB Author: Dr. Joseph Mercola, Dr. Kendra Degen Pearsall Narrator: Dave Clark
The FDA and worldwide current good manufacturing practices and quality system requirements guidebook for finished pharmaceuticals By Rodríguez Pérez, José 2014 | 369 Pages | ISBN: 0873898699 | PDF | 11 MB
New Drugs: An Insider's Guide to the FDA's New Drug Approval Process for Scientists, Investors and Patients by Lawrence T. Friedhoff English | 2009 | ISBN: 141969961X | 258 pages | EPUB + MOBI | 0,6 + 1,1 MB
New Drugs: An Insider's Guide to the FDA's New Drug Approval Process for Scientists, Investors and Patients by Lawrence T. Friedhoff English | 2009 | ISBN: 141969961X | 258 pages | EPUB + MOBI | 0,6 + 1,1 MB
Development of FDA-Regulated Medical Products: A Translational Approach, Second Edition By Whitmore, Elaine 2012 | 255 Pages | ISBN: 0873898338 | PDF | 6 MB
How to Develop and Manage Qualification Protocols for FDA Compliance by Phil Cloud English | Aug 31, 1999 | ISBN: 1574910981 | 371 Pages | PDF | 12 MB
All current Good Manufacturing Practices (cGMP), Good Clinical Practices (GCP), Good Laboratory Practices (GLP) and ISO 9000 standards and regulations require that validation document be established and followed. Yet these regulations do not provide guidelines on how to produce documentation such as qualification protocols.