Intelligent drug development : trials and errors in clinical research /

Clinical research is heavily regulated and involves coordination of numerous pharmaceutical-related disciplines. Each individual trial involves contractual, regulatory, and ethics approval at each site and in each country. Clinical trials have become so complex and government requirements so stringe...

Full description

Saved in:
Bibliographic Details
Author / Creator:Tansey, Michael, author.
Imprint:Oxford ; New York : Oxford University Press, [2014]
Description:1 online resource (241 pages)
Language:English
Subject:Clinical trials -- Ethics.
Clinical trials -- Methods.
Drug approval -- Methods.
Medical protocols.
Drug Approval -- methods.
Clinical Protocols.
Clinical Trials as Topic -- ethics.
Clinical Trials as Topic -- methods.
MEDICAL -- Pharmacology.
Medical protocols.
Clinical trials.
Drug approval.
Electronic books.
Methods (Music)
Format: E-Resource Book
URL for this record:http://pi.lib.uchicago.edu/1001/cat/bib/11754369
Hidden Bibliographic Details
ISBN:9780190200657
0190200650
9780199974580
0199974586
Notes:Includes bibliographical references (pages 213-215) and index.
Print version record.
Summary:Clinical research is heavily regulated and involves coordination of numerous pharmaceutical-related disciplines. Each individual trial involves contractual, regulatory, and ethics approval at each site and in each country. Clinical trials have become so complex and government requirements so stringent that researchers often approach trials too cautiously, convinced that the process is bound to be insurmountably complicated and riddled with roadblocks. A step back is needed, an objective examination of the drug development process as a whole, and recommendations made for streamlining the proces.
Other form:Print version: Tansey, Michael. Intelligent Drug Development. Oxford : Oxford University Press, 2014 9780199974580