Pharma & Life Sciences
Adverse Event Reporting
Process adverse event reports by extracting data from intake sources and entering into legacy safety databases for regulatory submission.
PharmacovigilanceIn Production
How It Works
1
Receive AE reports from HCPs, patients, literature, or trials
2
Extract relevant medical and product information
3
Navigate the safety database and create or update case records
4
Code events using MedDRA, assess causality, and prepare forms
What This Enables
Meets regulatory reporting timelines (15-day expedited, periodic)
Ensures consistent MedDRA coding and causality assessment
Handles intake volume spikes during safety signals
Ready to automate adverse event reporting?
Customers go from zero to production in 3 weeks. See how Minicor can automate this workflow for your EHR.
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