I'm looking for information about

Can't find what you're looking for? You may need to login to see more documents

AHRQ: Mandatory Use of Data Safety and Monitoring Plans
Exempt Human Subjects Research
Specialty Informed Consent Templates
Statement of Practice: Remote Study Procedures
Humanitarian Use Device Requirements for U-M Physicians & Investigators
Evaluating Risks to Participants
Privacy and Confidentiality Protections for Individual-Level Data Policy
Retention of Research Data/Biospecimens
Non-Significant Risk (NSR) Medical Devices: Monitoring Requirements
Emergency Research (Planned and Approved) with Exception from Informed Consent
G
Guidance
Suggested parameters and sets of instructions outlining best practices and standards for accomplishing specific duties.

Exempt Human Subjects Research

Updated on:

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

Evaluating Risks to Participants

Updated on:

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

Retention of Research Data/Biospecimens

Updated on: