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Research Institute : Clinical Research Administration : Information for Investigators/Study Coordinators

Investigator's Responsibilities

1572 Responsibilities (MS Word)
Good Clinical Practice in FDA Regulated Clinical Trials
Code of Federal Regulations (CFR)

a. Investigational New Drugs - 21 CFR Part 312
b. Investigational New Drug Responsibilities of Investigators - 21 CFR Part 312.60-312.70
c. Financial Disclosure by Clinical Investigators - 21 CFR Part 54
d. Investigational Device Exemptions - 21 CFR Part 812
e. Protection of Human Subjects - 21 CFR Part 50
Common Rule, Protection of Human Subjects, Federal Register 45 Part 46
FDA Information Sheets

This page last updated: October, 12, 2008

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Medical Center
Research Institute
6003 Wescoe Pavilion
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3901 Rainbow Boulevard
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Phone: 913-588-1249
Fax: 913-588-5729
E-Mail: cra@kumc.edu

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