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, Increasing number of Cases to be processed on a daily basis.
Manual data entry and coding of case-related information.
Fast-changing regulatory requirements and integration to safety database.
A pharmacovigilance process automation pipeline that automates case loading and case processing for varied document types.
Botminds AI crawlers automatically loaded the case documents for auto-classifying and auto-extracting the PV related information.
A one-stop automation solution to onboard any document type in minimal hours for end-to-end PV process.
See Botminds Unified platform in action