Advertisements Guidance |
FDA Inspection Readiness Guidance |
Prisoner Research Guidance |
Audiovideo Recording Guidance |
Glossary of IRB Terms |
Protocol Content Guidance |
Certificate of Confidentiality Guidance |
Good Clinical Practice Guidance |
Protocol Deviation or Violation Guidance |
CITI Training for Human Subject Research Guidance |
HIPAA and PHI Guidance |
Quality Control and Quality Improvement Guidance |
Clinical Research and Trial Management Tool Guidance |
Human Genetic Research Guidance |
Recordkeeping Guidance |
Clinical Trials.gov Registration Guidance |
Humanitarian Use Device Exemption Guidance |
Reporting Unanticipated Problems Guidance |
Closure of Studies or Submitting Final Report Guidance |
Individual Investigator Agreement Guidance |
Research Misconduct Guidance |
Conflict of Interest Guidance |
Non-Compliance Guidance |
Roles and Responsiblities of Investigators Guidance |
Consent Form and Procedures for Consenting Guidance |
OHRP Guidance on Elimination of Review of Research Grants and Proposals |
Surrogate Consent Guidance |
Consent Forms Guidance |
Pedagogy, Methodology and Classroom Teaching Guidance |
Tissue Collection, Repository, Private Identifiable Information and Data Bank Guidance |
Consenting Non-English Speaking Subjects Guidance |
Preparatory to Research Guidance |
Title IX Reporting Exception for Human Subjects Research |
Data Safety Monitoring Guidance |
Principal Investigator Definition and Qualification Guidance |
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Emergency Use of Test Article Guidance |
Principal Investigator Responsibilities Guidance |
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