Skip to main content
Sign In

University of Colorado Denver

 

LINKS

Clinical Research Education and Quality Assurance


Investigator Responsibilities and Information

Guidance for Industry Investigator Responsibilities Protecting the Rights, Safety, and Welfare of Study Subjects

Guidance for Clinical Investigators, Sponsors, and IRBs Adverse Event Reporting to IRBs Improving Human Subject Protection
 
 
 
 
"Off-Label" and Investigational Use Of Marketed Drugs, Biologics, and Medical Devices - Information Sheet Guidance for Institutional Review Boards and Clinical Investigators
 
Educational Materials - Useful References
 
INDs
Guidance for Industry Investigational New Drug Applications (INDs) Determining Whether Human Research Studies Can Be Conducted Without an IND
 
 
 
 
Institutional Review Boards Frequently Asked Questions - Information Sheet Information Sheet - Guidance for Institutional Review Boards and Clinical Investigators
 
University of Colorado Denver

© The Regents of the University of Colorado, a body corporate. All rights reserved.

All trademarks are registered property of the University. Used by permission only.