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Building Better Clinical Trials through Stewardship and Transparency September 16, 2016 (Extramural Nexus Blog)
Progress Reports and General Policies
- NIH Grants Policy Statement (NIH)
- Progress Reports
- NIH Form for Progress Reports (Revised 06/2009)
- Revised PHS 2590 (DHHS Public Health Service Noncompeting Continuation Progress Report) Now Available-Policy Changes Implemented
- New Requirement for eRA Commons User IDs for Individuals in a Postdoctoral Project Role with Measurable Effort on an NIH Annual Progress Report (PHS2590)
- Funding Acknowledgement Requirement
For publishing or presenting research findings - NIH Policy Notices (NIH)
- Data Sharing Policy (NIH)
- Rigor and Reproducibility (NIH)
- Public Access Policy (NIH)
- What NIH Grantees Need to Know about ClinicalTrials.gov and FDAAA (NIH)
- International Interventional Clinical Studies: NCCIH Special Considerations
- Applications Requesting Direct Costs of $500,00 or More in Any One Year (NCCIH Policy)
Natural Products Research
- Natural Product Integrity Policy—Researchers must submit specific product information to NCCIH
Share Your Research:
Tips for Working With the Media
Data and Safety Monitoring
- Data and Safety Monitoring of NCCIH-Funded Clinical Research
- NIH Policy on Data and Safety Monitoring Boards (NIH)
- Data and Safety Monitoring for Phase I and Phase II Trials (NIH)
- Data and Safety Monitoring: Frequently Asked Questions (NIH)
Human Subjects and Animal Protection
- NCCIH Clinical Terms of Award for Human Subjects Research
- NIH Single IRB (sIRB) Policy
- Office for Human Research Protections (HHS)
- Certificates of Confidentiality (NIH)
- Required Education in the Protection of Human Research Participants (NIH)
- Guidance on Changes That Involve Human Subjects in Active Awards and That Will Require Prior NIH Approval (NIH)
- FAQ on Required Education in the Protection of Human Research Participants (NIH)
- Office of Animal Care and Use (NIH)