Workshop 3: Pharmacovigilance Inspections/audits readiness and procedures to manage these, AND Maintain product safety committee/board operational
PATH & DCVMN consultant
1. Documentation and record management
2. Compliance monitoring and system performance
3. Critical pharmacovigilance processes and business continuity
Pre-reading material
https://www.ema.europa.eu/en/documents/scientific-guideline/guideline-good-pharmacovigilance-practices-module-i-pharmacovigilance-systems-their-quality-systems_en.pdf
