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Clinical Trials Network
Good Clinical Practice
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Module Content - To View Offline or for Printing
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Introduction
Institutional Review Boards
Informed Consent
Confidentiality & Privacy
Participant Safety & Adverse Events
Quality Assurance
The Research Protocol
Documentation & Record-Keeping
Research Misconduct
Roles & Responsibilities
Recruitment & Retention
Investigational New Drugs
Introduction
Institutional Review Boards
Informed Consent
Confidentiality & Privacy
Participant Safety & Adverse Events
Quality Assurance
The Research Protocol
Documentation & Record-Keeping
Research Misconduct
Roles & Responsibilities
Recruitment & Retention
Investigational New Drugs
Additional Resources
NIDA CCTN Clinical Trials Network
Conferences/Meetings
CTN Dissemination Library
CTN Training Suggestion Box
Network Updates
Training Sessions and Webinars
ClinicalTrials.gov
NIDA Clinical Coordinating Center
NIH Certificates of Confidentiality Kiosk (For non-IND studies)
NIH Training on Protecting Human Research Participants
U.S. DHHS
Office of Human Research Protections (OHRP)
Federalwide Assurance (FWA)
U.S. DOJ Drug Enforcement Administration (DEA)
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