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• About COUHES
  • Dates & Deadlines
  • Members & Staff
  • Contact Us
• For Researchers
  • COUHES 101
  • Definitions
    • Engaged in Research: Scenarios
  • Policies & Procedures
    • Audit
    • Continuing Review
    • Criteria for Acceptance of Studies
    • Financial Conflicts of Interest
    • Guidance on NIH Genomic Data Sharing (GDS) Policy
    • Ongoing Monitoring and Reporting
    • Principal Investigator Status
    • Record Keeping
    • Research at Collaborating Institution
    • Review and Approval of Studies
    • Sabbaticals and Leaves of Absence
    • Training of Research Personnel
  • Guidelines
    • Additional Review (China, Russia or Saudi Arabia)
    • Adult Subjects with Cognitive Impairment and Reduced Decision-Making Capacity
    • Artificial Intelligence (AI) in Research
    • Audiotaping and Videotaping
    • COUHES Policy for Using Amazon's Mechanical Turk
    • Data Handling When a Subject Withdraws From a Study
    • Data Protection
    • Data Sharing
    • Electronic Consent
    • FDA Regulated Research
    • General Data Protection Regulation (GDPR) and Research Activities
    • Guidance on Use of Protected Health Information for Research Purposes
    • Guidelines for Single IRB
    • Guidance for Student Research and Class Projects
    • Including Women of Childbearing Potential in Research and Pregnancy Testing
    • Minors
    • MIT Students and Lab Members as Subjects
    • MRI and Pregnancy
    • Non-English Speakers
    • Oral History Activities
    • Other Vulnerable Subjects
    • Passive Parental Consent
    • Payment and Costs
    • Pregnant Women
    • Private Data, Human Specimens and Cells
    • Research Involving Deception
    • Research Involving Mental Health Topics
    • Research Involving Non-MIT Collaborators
    • Research that May Affect Privacy of Health Information
    • Students as Subjects
    • Subjects with Limited Ability to Read, Hear, or See
    • Subjects with Limited Comprehension
    • Surveys, Questionnaires and Interviews
  • Informed Consent
    • Additional Standard Language for Informed Consent
    • Basic Elements of Informed Consent
    • Waiver or Alteration of Informed Consent or Waiver of Documentation of Informed Consent
  • Clinical Trials at MIT
    • Certificates of Confidentiality
    • ClinicalTrials.gov Requirements
    • Data Safety Monitoring Plan (DSMP)
    • GCP Training
  • FAQ
  • COUHES Connect Resources
    • COUHES Connect FAQs
    • COUHES Connect Guidance
    • Helpful Links
  • Department of Defense (DoD) Sponsored or Supported Exempt Research
  • HIPAA Guidance Document
• Forms & Templates
• Education and Training
  • GCP Training
  • Human Subjects Training (HST)
    • HST FAQs
    • HST Notifications
    • HST Reports
• Single IRB Review
  • Single IRB Review FAQs
• Announcements