Regulation of medicines & medical devices books

"Discussing the role biosensors play in detecting and monitoring environmental substances, Biosensors and Environmental...  Read More >>

Cyberpop is an analysis of cyberculture and its popular cultural productions, looking at film, art, advertising...  Read More >>

“Patenting Nanomedicines: Legal Aspects, Intellectual Property and Grant Opportunities” focusses on the fundamental...  Read More >>

Drug & Device Product Liability Litigation Strategy provides useful practice pointers and overall strategic guidance...  Read More >>

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This study, by two leading scholars in the field, draws on feminist theory and science and technology studies to...  Read More >>

A gripping blockbuster account of an American icon, the most lucrative biotech drug ever, $11 billion in global...  Read More >>

A gripping blockbuster account of an American icon, the most lucrative biotech drug ever, $11 billion in global...  Read More >>

As the practice of modern medicine becomes more and more pharmacology dependent, the role of pharmacy technicians...  Read More >>

Opening with a detailed account of the historical development of Irish pharmacy and medicines law, this practical...  Read More >>

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The US Food and Drug Administration is the most powerful regulatory agency in the world. How did the FDA become...  Read More >>

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 >>

This book demonstrates how the Thalidomide catastrophe of the 1960s and the BSE crisis of the 1990s led to regulatory...  Read More >>

A scientific technical code on the quality of medicinal products is essential for a statute on medicines. That code...  Read More >>

Cyberpop is an analysis of cyberculture and its popular cultural productions, looking at film, art, advertising...  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 >>

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Luminescent Thermometers deals with all the aspects of the subject from principles of methods to their applications...  Read More >>

The book is designed to help medical device manufacturers navigate FDA regulation, carefully consider the parameters...  Read More >>