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Clinical Trials with No/Low Enrollment: Guide for Departments
Specialty Informed Consent Templates
Statement of Practice: Remote Study Procedures
Evaluating Risks to Participants
Single IRB (sIRB) and Cooperative Multi-Site Research
IRBMED Review Fees
Guidelines for Studies Conducted Through MCOHR and the Dental School
Non-Significant Risk (NSR) Medical Devices: Monitoring Requirements
Protocol Resources
Information Blocking in a Blinded Study
G
Guidance
Suggested parameters and sets of instructions outlining best practices and standards for accomplishing specific duties.

Evaluating Risks to Participants

Updated on:

I
Informational
Informational tools to help guide you through specific tasks.

IRBMED Review Fees

Updated on:

G
Guidance
Suggested parameters and sets of instructions outlining best practices and standards for accomplishing specific duties.

Protocol Resources

Updated on:

G
Guidance
Suggested parameters and sets of instructions outlining best practices and standards for accomplishing specific duties.

Information Blocking in a Blinded Study

Updated on: