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Category A
Adverse Event & Deviation Reporting
Structured reporting module for serious adverse events and protocol deviations.
Service Facts
Estimated Time
24–72 hours
Pricing / Estimate
Included in all plans
Target Group
PIs, Research Nurses, Coordinators
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Service Overview
Structured reporting module for serious adverse events (SAEs), unanticipated problems, and protocol deviations. Automated escalation workflows with regulatory notification timelines.
Key Capabilities
- Submission confirmation
- Event tracking number
- Regulatory notification draft
- Corrective action log