AI Agents for Life Sciences Pharmacovigilance
AI agents for life sciences pharmacovigilance intake adverse event reports from email, forms and partners, check them for completeness, extract case data and prepare each case for safety review and reporting. Safety teams spend their time on medical assessment, not on data entry and chasing follow-up information.
Where Pharmacovigilance Case Processing Breaks Down
Safety teams receive adverse event reports in many formats and enter the data into the safety database by hand before assessment can begin.
AI Agents Built for Every Pharmacovigilance Workflow
Six connected capabilities designed around your safety database, case processing procedures and reporting rules for Life Sciences teams.
- Receives adverse event reports from email, forms, call notes and partner exchanges
- Classifies each item as a potential case, follow-up or non-case
- Records receipt date and source for every item
- Creates a case record for review
- Routes items to the right queue
- Extracts patient, product, event, dose and reporter details from documents
- Maps terms to your coding conventions for review
- Flags unreadable or ambiguous values for each case
- Keeps the source linked to each field
- Prepares the entry for the safety database
- Checks each case for the minimum information your procedures require
- Lists missing data for follow-up
- Drafts follow-up requests for the case processor to send
- Tracks follow-up responses
- Flags cases that remain incomplete
- Compares new cases with existing cases on key fields
- Flags possible duplicates with the matching fields shown
- Leaves the merge decision to the case processor
- Links related reports to the same case
- Records the decision
- Calculates reporting due dates from receipt date and seriousness under your rules
- Alerts owners as clocks approach
- Shows cases by due date and status
- Flags cases at risk of missing a clock
- Keeps history of the dates used
- Prepares safety data exchange files for partners from approved cases
- Reconciles received and sent cases with partners
- Flags cases missing on either side
- Tracks acknowledgements
- Keeps exchange records for review
How We Deploy Your Pharmacovigilance Agent
Five steps from your first call to a validated pharmacovigilance workflow connected to your safety database.
The right case visibility for every safety role
Each deployment is scoped around how a specific role depends on adverse event data. Case processors, safety physicians and quality leaders each get the outcome they need.
- Reports classified and logged on receipt
- Case data extracted with the source linked
- Missing information listed for follow-up
- Possible duplicates flagged
- Case summary with source documents attached
- Completeness status shown
- Seriousness and clock status visible
- Medical assessment left to you
- Cases by due date and risk of missing a clock
- Follow-up status by case
- Partner exchange reconciliation
- Record of dates and decisions
Questions About Pharmacovigilance Automation
What case processors, safety physicians and quality leads ask before the first call.
Ready to Stop Keying Adverse Event Cases?
Book a discovery call to walk through your intake channels, your case procedures and your safety database.
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