Übersicht			Auf mobile öffnen

Lieferstatus:	Auf Bestellung (Lieferzeit unbekannt)
Veröffentlichung:	Oktober 1993
Genre:	Naturwissensch., Medizin, Technik
	adverse event monitoring / clinical data management / ethics committee approval / European clinical trial legislation / investigational product oversight / MEDICAL / Pharmacology / pharmaceutical research methods / Pharmacology / regulatory compliance processes mehr...
ISBN:	9781857750355
EAN-Code:	9781857750355
Verlag:	Taylor and Francis
Einband:	Kartoniert
Sprache:	English
Dimensionen:	H 216 mm / B 138 mm / D
Gewicht:	210 gr
Seiten:	124
Bewertung:	Titel bewerten / Meinung schreiben

Inhalt:

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.