Grantee Policies and Resources
Important information and procedures for investigators who have been awarded grants.
Progress Reports and General Policies
- 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 - NCCAM Terms of Awards for Clinical Trials
- NCCAM Clinical Research Toolbox
- NIH Grants Policy Statement (NIH)
- NIH Policy Notices (NIH)
- Data Sharing Policy (NIH)
- Public Access Policy (NIH)
- What NIH Grantees Need to Know about ClinicalTrials.gov and FDAAA (NIH)
Data and Safety Monitoring Boards
- Data and Safety Monitoring of NCCAM-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
- Certificates of Confidentiality (NIH)
- Office for Human Research Protections (HHS)
- 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)
Natural Products Research
- Natural Product Integrity Policy—Researchers must submit specific product information to NCCAM