Submit Adverse Event Report from an Electronic Health Record to Drug Safety Regulators

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Type Standard Implementation/Specification Standards Process Maturity Implementation Maturity Adoption Level Federally required Cost Test Tool Availability
Implementation Specification
Final
Production
Rating 4
No
Free
N/A
Implementation Specification
Balloted Draft
Pilot
Rating 1
No
Free
N/A
Implementation Specification
Balloted Draft
Production
Rating 2
No
Free
N/A
Limitations, Dependencies, and Preconditions for Consideration Applicable Security Patterns for Consideration
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remove this entry from the table. PRM is not closely related to adverse event submission.