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Specialty Informed Consent Templates
Retention of Research Data/Biospecimens
Non-Significant Risk (NSR) Medical Devices: Monitoring Requirements
Statement of Practice: Document Revision Guidance, Naming Convention, and Version Control
Protocol Resources
G
Guidance
Suggested parameters and sets of instructions outlining best practices and standards for accomplishing specific duties.

Retention of Research Data/Biospecimens

Updated on:

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

Protocol Resources

Updated on: