How To Develop A Productive Morning Routine Q A For Professionals
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Good Clinical, Laboratory and Manufacturing Practices
Author: Philip Carson
language: en
Publisher: Royal Society of Chemistry
Release Date: 2007-10-31
Quality assurance and good laboratory practices are becoming essential knowledge for professionals in all sorts of industries. This includes internal and external audit procedures for compliance with the requirements of good clinical, laboratory and manufacturing practices. Spanning chemical, cosmetic and manufacturing industries, Good Clinical, Laboratory and Manufacturing Practices: Techniques for the QA professional is aimed at: chemists, clinicians, ecotoxicologists, operation managers, pharmaceutical process managers, quality assurance officers, technicians and toxicologists. In addition sections on harmonisation of quality systems will be of value to safety, health and environment advisors. This comprehensive and high level reference will be an indispensable guide to research laboratories in academia and industry. Additional training material is also included.
Principles and Practice of Pharmaceutical Medicine
Author: Lionel D. Edwards
language: en
Publisher: John Wiley & Sons
Release Date: 2011-07-12
The new edition of Principles and Practice of Pharmaceutical Medicine is a comprehensive reference guide to all aspects of pharmaceutical medicine. New content includes chapters and coverage on regulatory updates, increasing international harmonization, transitional and probabilistic approaches to drug development, the growing sophistication and regulatory importance of pharmacovigilance, personalized medicine and growth in biotechnology as a source of new experimental drugs.
Good Clinical, Laboratory and Manufacturing Practices
Author: Phillip A. Carson
language: en
Publisher: Royal Society of Chemistry
Release Date: 2007
Provides practical advice for the quality assurance professional responsible for monitoring compliance with legal requirements and accepted standards of preclinical safety studies, clinical trials and manufacture of drugs. This book also offers a framework for integrating these standards with other quality management systems.