Rock solid data and AI governance for clinical safety and Pharmacovigilance

Regulatory agencies expect a complete, traceable record of Adverse Events (AEs) from pharma and life sciences: every governance decision and every downstream transformation of safety data, from source system to health authority submission documented.

Collibra creates a centralized inventory of priority Clinical Safety and Pharmacovigilance (CSPV) datasets, systems, reports, and external data sources — with ownership, metadata, and business glossary definitions.