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Tips on the REP Application and Supplement Form
Repository Overview
Evaluation, Screening and Diagnostic Testing for Determination of Clinical Trial Eligibility
External Adverse Event (AE) Reporting
eResearch Regulatory Management (eRRM)
Unanticipated Problems Involving Risks to Subjects or Others
Who May Consent for Participation in Research Studies (Michigan)
Investigator Responsibilities

Guidance

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

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

Repository Overview

Updated on:

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

External Adverse Event (AE) Reporting

Updated on:

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

eResearch Regulatory Management (eRRM)

Updated on:

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

Investigator Responsibilities

Updated on: