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COUHES 101
Definitions
Policies & Procedures
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Informed Consent
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Department of Defense (DoD) Sponsored or Supported Exempt Research
HIPAA Guidance Document
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Education and Training
Education and Training
This section contains training requirements and instructions pertaining to human subjects research.
Enter search text
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
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
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
