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163 books were found.
The US Food and Drug Administration is the most powerful regulatory agency in the world. How did the FDA become... Read More >>
Drug delivery systems represent a vast area of research and development within biomaterials and medicine and the... Read More >>
A guide to law and ethics for pharmacy practice in the UK. It discusses the law that affects the practice of pharmacy... Read More >>
The production of medicines - pharmaceutical and herbal - involves the sourcing of both genetic resources in the... Read More >>
Working with Government Agencies in Tax Law is an authoritative, insiders perspective on best practices for communicating... Read More >>
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A scientific technical code on the quality of medicinal products is essential for a statute on medicines. That code... Read More >>
Applies Six Sigma principles to the design of medical devices. This book provides a practical how-to guidance for... Read More >>
The module in the Global Assessment Programme (GAP) toolkit contains methodological guidance on the development... Read More >>
The book presents the latest advances in soft electronics in biomedical engineering and its potential applications... Read More >>
The book is designed to help medical device manufacturers navigate FDA regulation, carefully consider the parameters... Read More >>