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Clinical Trials
An Introduction
Taschenbuch von Ann Raven (u. a.)
Sprache: Englisch

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Beschreibung
This volume provides an introduction to the process of clinical drug development. It demystifies the way new medicines are discovered, tested and regulated. This book is intended for those who wich to understand the background of clinical trials from a pharmaceutical company perspective, and is suitable for clinical trials supplies technicians and pharmacists, data management staff, information officers, medical secretaries and all support staff. This second edition is updated and includes information on the practical implications of recent EC legislation.
This volume provides an introduction to the process of clinical drug development. It demystifies the way new medicines are discovered, tested and regulated. This book is intended for those who wich to understand the background of clinical trials from a pharmaceutical company perspective, and is suitable for clinical trials supplies technicians and pharmacists, data management staff, information officers, medical secretaries and all support staff. This second edition is updated and includes information on the practical implications of recent EC legislation.
Über den Autor
Ann Raven, Frank Wells
Inhaltsverzeichnis
1: Drug Development; 2: Regulation of Drug Research; 3: Good Clinical Practice; 4: Clinical Investigators; 5: Trial Design and Protocols; 6: Case Record Forms; 7: Trial Supplies; 8: Clinical Research Associates; 9: Monitoring and Adverse Events; 10: Analysis and Reports; 11: Standard Operating Procedures (SOPs), Audits and Archives
Details
Erscheinungsjahr: 1993
Fachbereich: Allgemeine Lexika
Genre: Importe, Medizin
Rubrik: Wissenschaften
Medium: Taschenbuch
ISBN-13: 9781857750355
ISBN-10: 1857750357
Sprache: Englisch
Einband: Kartoniert / Broschiert
Autor: Raven, Ann
Wells, Frank
Auflage: 2. Auflage
Hersteller: CRC Press
Verantwortliche Person für die EU: Books on Demand GmbH, In de Tarpen 42, D-22848 Norderstedt, info@bod.de
Maße: 216 x 140 x 7 mm
Von/Mit: Ann Raven (u. a.)
Erscheinungsdatum: 01.10.1993
Gewicht: 0,172 kg
Artikel-ID: 128465161
Über den Autor
Ann Raven, Frank Wells
Inhaltsverzeichnis
1: Drug Development; 2: Regulation of Drug Research; 3: Good Clinical Practice; 4: Clinical Investigators; 5: Trial Design and Protocols; 6: Case Record Forms; 7: Trial Supplies; 8: Clinical Research Associates; 9: Monitoring and Adverse Events; 10: Analysis and Reports; 11: Standard Operating Procedures (SOPs), Audits and Archives
Details
Erscheinungsjahr: 1993
Fachbereich: Allgemeine Lexika
Genre: Importe, Medizin
Rubrik: Wissenschaften
Medium: Taschenbuch
ISBN-13: 9781857750355
ISBN-10: 1857750357
Sprache: Englisch
Einband: Kartoniert / Broschiert
Autor: Raven, Ann
Wells, Frank
Auflage: 2. Auflage
Hersteller: CRC Press
Verantwortliche Person für die EU: Books on Demand GmbH, In de Tarpen 42, D-22848 Norderstedt, info@bod.de
Maße: 216 x 140 x 7 mm
Von/Mit: Ann Raven (u. a.)
Erscheinungsdatum: 01.10.1993
Gewicht: 0,172 kg
Artikel-ID: 128465161
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