Drugs between Research and Regulations: Proceedings of the 5th International Meeting of Pharmaceutical Physicians Munich, October 14–17, 1984
Editat de C. Steichele, U. Abshagen, J. Koch-Weseren Limba Engleză Paperback – 22 dec 2012
Preț: 693.12 lei
Preț vechi: 729.59 lei
-5% Nou
Puncte Express: 1040
Preț estimativ în valută:
132.66€ • 138.27$ • 110.44£
132.66€ • 138.27$ • 110.44£
Carte tipărită la comandă
Livrare economică 06-20 ianuarie 25
Preluare comenzi: 021 569.72.76
Specificații
ISBN-13: 9783642541322
ISBN-10: 3642541321
Pagini: 224
Ilustrații: XII, 206 p. 4 illus.
Dimensiuni: 170 x 244 x 15 mm
Greutate: 0.36 kg
Ediția:Softcover reprint of the original 1st ed. 1985
Editura: Steinkopff
Colecția Steinkopff
Locul publicării:Heidelberg, Germany
ISBN-10: 3642541321
Pagini: 224
Ilustrații: XII, 206 p. 4 illus.
Dimensiuni: 170 x 244 x 15 mm
Greutate: 0.36 kg
Ediția:Softcover reprint of the original 1st ed. 1985
Editura: Steinkopff
Colecția Steinkopff
Locul publicării:Heidelberg, Germany
Public țintă
Professional/practitionerCuprins
Chronic Concern on Chronic Toxicity Studies.- Chronic toxicity tests, current problems and possible solutions.- What can be gained from a retrospective analysis of chronic toxicity studies?.- The role of carcinogenicity studies in risk assessment.- Alternatives to chronic toxicity studies.- Clinical Trials and Medical Practice.- What good are clinical trials?.- Clinical guidelines — a help or a hindrance?.- Clinical trials in the natural environment.- Clinical trials and the general practitioner.- Clinical trials and chronic diseases.- Alternatives to clinical trials in post-marketing research on drug effects.- The Future of Long-Term Intervention and Prevention Studies.- The future of long-term intervention and prevention studies — methodological aspects.- Lessons for the future from long-term studies with beta blockers and hypolipidaemic agents.- Rauwolfia derivatives and breast cancer: how do we know when we have the answers?.- The organisation of long-term intervention and prevention studies.- New Biostatical Concepts for Clinical Trials.- The explanatory and pragmatic approaches in clinical trials.- Alternatives to classical randomized trials.- Data quality assurance with particular regard to protocol violations.- Clinical Trials in Children.- The need of clinical drug trials in children.- Ethical restrictions in clinical trials in children.- European Drug Registration.- The role of the EEC in the harmonisation of drug registration.- Clinical trials — European recommendations.- Special Lecture.- The Pharmaceutical Industry — research and responsibility.