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Seeking Reconsent from Research Participants
Study-Specific Adverse Event (AE) Reporting Plans
Adverse Events (AEs), Other Reportable Information and Occurrences (ORIOs), & Other Required Reporting
Adverse Event Reporting
Deception and Concealment
NIH Genomic Data Sharing Policy
University of Michigan Medical School Central Biorepository Policy Acknowledgment and Authorship
Tips on the REP Application and Supplement Form
Repository Overview
External Adverse Event (AE) Reporting
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.

Deception and Concealment

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:

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

External Adverse Event (AE) Reporting

Updated on: