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Study-Specific Adverse Event (AE) Reporting Plans
Statement of Practice: eResearch Cross-Reference Table
Statement of Practice: IRBMED Finalization of Study Documents
Statement of Practice: Ancillary Approval & Final IRBMED Approval
Adverse Events (AEs), Other Reportable Information and Occurrences (ORIOs), & Other Required Reporting
Adverse Event Reporting
UMMS Biorepository Registration Decision Tree
Data Office Data Request Form
Data Office Access Request Form
Data Office Data Set Specification

Topic: eResearch Regulatory Management (eRRM)

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

Adverse Event Reporting

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