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Protected Health Information (PHI)
Limited Data Sets
Uses & Disclosures of Protected Health Information (PHI)
Decedents
Seeking Reconsent from Research Participants
Study-Specific Adverse Event (AE) Reporting Plans
FAQ: Repository application (REP)
Adverse Events (AEs), Other Reportable Information and Occurrences (ORIOs), & Other Required Reporting
Adverse Event Reporting
UMMS Biorepository Registration Decision Tree

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.

Protected Health Information (PHI)

Updated on:

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

Limited Data Sets

Updated on:

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

Decedents

Updated on:

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

FAQ: Repository application (REP)

Updated on:

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

Adverse Event Reporting

Updated on: