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Regulation of Medical Products -

Regulation of Medical Products

John Griffin, John O'Grady (Herausgeber)

Buch | Softcover
310 Seiten
2003
BMJ Books (Verlag)
978-0-7279-1780-5 (ISBN)
CHF 108,15 inkl. MwSt
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A concise but comprehensive text explaining the processes involved in regulation of drugs with particular emphasis on EU, USA and Australia.

John Griffin is the editor of Regulation of Medical Products, published by Wiley. John O'Grady is the editor of Regulation of Medical Products, published by Wiley.

Contributors. Preface.

Acknowledgements.

The Editors.

History of drug regulation in the UK.

Regulation of human medicinal products in the European Union.

European regulation of medical devices.

The supply of unlicensed medicines for particular patient use.

Controls on NHS medicines prescribing and expenditure in the UK (a historical perspective).

The regulation of therapeutic products in Australia.

Regulatory and clinical trial systems in Japan.

The regulation of drug products by the United States Food and Drug Administration.

The US FDA in the drug development, evaluation, and approval process.

Technical requirements for registration of pharmaceuticals for human use: the ICH process and the Common Technical Document.

Appendix: European guidelines relevant for pharmaceutical physicians.

Index

Erscheint lt. Verlag 3.4.2003
Sprache englisch
Maße 158 x 236 mm
Gewicht 481 g
Themenwelt Medizin / Pharmazie Medizinische Fachgebiete Pharmakologie / Pharmakotherapie
Medizin / Pharmazie Pharmazie
Technik
ISBN-10 0-7279-1780-3 / 0727917803
ISBN-13 978-0-7279-1780-5 / 9780727917805
Zustand Neuware
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