Automated end-to-end pharmacovigilance process - managing multiple reporting templates, source and changing regulatory requirements
A large global pharmaceutical company headquartered in USA with products marketed across the globe.
Manually identifying, downloading multiple sources and document formats.
Scarce Subject Matter Expertise, Cases to be processed is increasing in daily basis.
Manual data entry & coding of case related information.
Fast-changing Regulatory Requirements and Integration to Safety Database.
A PV process automation pipeline that automates the Pharmacovigilance case loading and case processing for the varied document types.
Case documents were automatically loaded by Botminds AI crawlers that we're able to auto classify and auto-extract the PV related information.
A one-stop automation solution to onboard any new document type with minimal hours for end-to-end PV process.
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