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Adverse Event Reporting
UMMS Biorepository Registration Decision Tree
Expedited Review
Deception and Concealment
FDA Expanded Access Program at the University of Michigan
Clinical Research Billing Guidance (CRB)
NIH Genomic Data Sharing Policy
Tips on the REP Application and Supplement Form
Responsibility for REP Oversight and Compliance
Repository Overview

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.

Adverse Event Reporting

Updated on:

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

Expedited Review

Updated on:

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

Deception and Concealment

Updated on:

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

Clinical Research Billing Guidance (CRB)

Updated on:

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

NIH Genomic Data Sharing Policy

Updated on:

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

Repository Overview

Updated on: