Ch. 1. Rules, roles, and responsibilities -- ch. 2. Products, protocols, and pretrial preparation -- ch. 3. Sponsor, site, and study start-up -- ch. 4. Enticement, enrollment, and engagement : the informed consent process -- ch. 5. From enrollment to final visit -- ch. 6. Collaborating for compliance and quality data : monitoring and audits -- ch. 7. Building budgets -- ch. 8. Contracts, clauses, and closing the deal -- ch. 9. U.S. clinical trials : additional topics -- ch. 10. Clinical research and India.
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OTHER EDITION IN ANOTHER MEDIUM
International Standard Book Number
9781138196506
TOPICAL NAME USED AS SUBJECT
Clinical trials-- Management, Handbooks, manuals, etc.