ClaroPV offers comprehensive and proficient support for pre-approval and post-market Pharmacovigilance (PV) and Medical Information (MI) services across various categories of medical products, including pharmaceutical drugs (both brand and generic), biologics, radiopharmaceutical drugs, natural health products, and medical devices.​ Our services include set-up of PV systems and processes​, preparation of PV agreements​, GVP audits and gap analysis (vendors, contractual partners, self-inspections)​, GVP inspection readiness, PV training, ICSR processing​, aggregate reporting, signal detection and management​, risk management planning, literature screening​, foreign action monitoring and notification​, and screening of Canada Vigilance, and call centre/medical information provision.