Pr-041904 Use of Electronic Signatures for Essential Documents in Clinical Research
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Type
Presentation
Credit
No
Description
Emphasizes the importance of data integrity, accountability, and security when transitioning from traditional ... show more
Objectives
- Regulated by the Food and Drug Administration (FDA), e-signatures must meet specific criteria, such as those outline in FDA 21 CFR Part 11 [Procedure MG.O-004.12]
Fees
Free
Faculty
Candice Vance
Organization
MedStar Health Research Institute