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OverviewFull Product DetailsAuthor: Steve WilliamsPublisher: Elsevier Science & Technology Imprint: Woodhead Publishing Ltd Volume: No. 31 ISBN: 9781907568503ISBN 10: 1907568506 Pages: 250 Publication Date: 01 October 2012 Audience: Professional and scholarly , College/higher education , Professional & Vocational , Undergraduate Format: Hardback Publisher's Status: Out of Stock Indefinitely Availability: Awaiting stock ![]() Table of ContentsReviewsAuthor InformationSteve Williams is Senior Partner and Director - International Education SeerPharma Pty Ltd, Australia. Steve has over 38 years experience in the biotechnology, pharmaceutical and medical device industries in quality assurance, manufacturing and consulting. He has conducted numerous FDA and EU/TGA/PICs compliance audits and gap analysis for many international companies as well as developed multiple training courses in GMP, GLP, validation, risk management, sterile manufacture, HACCP and medical device regulations. Steve regularly presents at conferences and industry seminars on a range of subjects relating to QA, risk management and GMP compliance. He also specialises in e-learning and compliance training solutions for the life sciences industry. Steve has successfully prepared multiple companies for FDA, EU, TGA, and PICS regulatory inspections over the last 20 years and has provided expert reports in GMP compliance for regulatory agencies and courts. He is also a registered auditor for the Australian Pesticides and Veterinary Manufacturing Authority (APVMA) and, in this role, conducts GMP licensing audits on behalf of the Australian government. Tab Content 6Author Website:Countries AvailableAll regions |