The Anna Maria Program has incorporated advice from federal authorities, feedback from research ethics leaders, and a great deal of best practices from other academic institutions into its policies and guidelines. The knowledge contained in these guidelines documents is based on concepts that are openly exchanged amongst institutions and is made possible by the professionalism and generosity of the community of experts in the field of human research safeguards.
Guidance for Researchers
Guidance
- ClinicalTrials.gov Registration & Reporting Requirements
- Consent
- Data Security
- Deception
- Department of Defense
- Drugs, Biologics, and Dietary Supplements
- Exercise Testing
- Glossary of Research Related Terms
- Graduate School Policy on IRB Approval
- International Research
- Letters of Support from External Sites of Recruitment or Research
- Medical Devices
- Public Schools
- Race and Ethnicity
- Recruitment of Research Participants
- Snowball Sampling
- Students and Employees as Research Participants
- Tribal Populations
Decision Tree
- Data Security (pdf)
- Engagement in Research (pdf)
- FDA
- Research Involving Human Subjects under FDA regulations (pdf)
- Investigational New Drug (IND) (pdf)
- Medical Devices
- FERPA Applicability to Research (pdf)
- Obtaining Parental Permission (pdf)
- Protection of Pupil’s Rights Amendment (PPRA) Applicability to Research (pdf)
- Research Involving Human Subjects (pdf)
Other Resources
- Office for Human Research Protections (OHRP)
- DHHS Policy for IRB Review of Applications for HHS Support
- HIPAA
- Data and Safety Monitoring (NIDDK)
- NIH Policy for IRB Review of Human Subjects Protocols in Grant Applications
- Investigator Responsibilities (OHRP)
- Inclusion of Women and Minorities (NIH)
- International Compilation of Human Subject Research Protections (OHRP)
- ClinicalTrials.gov