- SOP for Search and Review of Global Medical Literature and Digital Media to Identify adverse events and Safety Data
- SOP for Handling of Adverse events and Safety Information
- SOP for Handling of Medical Inquiries
- SOP for Safety Data Exchange Agreements
- SOP for Communication of Safety Concerns to Consumers HCP’s and Regulatory Authorities
- SOP for Implementation of Safety Variations in Product’s Labeling Documents
- SOP for Risk Management Plan
- SOP for Periodic Safety Update Report (PSUR)
- SOP for Signal Management
- SOP for Pharmacovigilance Audit & Inspection Readiness
- SOP for Pharmacovigilance System Master File (PVMF)