Outsourcing in Clinical Drug Development
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biostatistics in medicine
Category=PS
Chronic
Clinical CROs
Clinical Data Management
clinical trial operations
CMR
Common Technical Document
company
contract
Core Competence
CRO
CRO Industry
CRO Performance
CRO Staff
CRO's Service
CRO’s Service
Cts
Drug Development
eq_bestseller
eq_isMigrated=1
eq_isMigrated=2
eq_nobargain
eq_non-fiction
eq_science
GCP
global clinical research partnerships
good
Ich GCP
laboratory outsourcing ethics
management
organizations
pharmaceutical
pharmaceutical project management
Ppd
PRA
regulatory compliance strategies
research
site
SMOs
Sourcing Decision
Sponsor Company
strategic
Strategic Outsourcing
supplier evaluation methods
Tactical Outsourcing
trial
Vice Versa
Violate
White Cell
Product details
- ISBN 9781574911121
- Weight: 660g
- Dimensions: 178 x 254mm
- Publication Date: 15 Aug 2002
- Publisher: Taylor & Francis Inc
- Publication City/Country: US
- Product Form: Hardback
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Sponsor companies and CROs alike will appreciate the industry-wide analysis, practical, how-to advice, and helpful charts and checklists provided by Outsourcing in Clinical Drug Development. A panel of experts discuss supplier identification and selection, financial considerations, and the ethical issues. They cover contracting out laboratory analysis, data management, and statistical services, and the effects of outsourcing on quality assurance. Whether readers are beginning to explore the possibility of outsourcing or already involved in long-term strategic outsourcing partnerships, this invaluable resource is a complete guide to the drug development outsourcing relationship.
Roy Drucker, Graham Hughes
