The PVG Pharmasciences team has core competency in creating PSMF, PSMF summary (CTD Module 1.8.1) and supporting documents for applicable submission for the nations with PSMF requirements.

Even when PSMF standards aren’t required, it’s always a good practice to document the whole working system for safety-related procedures (i.e., detailed description of Market Authorization Holder’s Pharmacovigilance System). We support our customers with precise documentation of all existing drug safety-related procedures.