Pharmaco Vigilance We cover a wide range of areas regarding safety and pharmacovigilance in Japan: Strategic Advice and Operational Support on any aspect related to safety and pharmacovigilance in Japan Assessment and Review of safety documents (Module 1, Module 2, RMP, etc.) for submissions to PMDA Gap Analysis of global documents to meet Japan-specific requirements Preparation and Review of SOPs for GVP (Good Vigilance Practice) and GPSP (Good Post-marketing Study Practice) Consultation and Interactions with PMDA regarding safety matters Strategy and Management of PMS, EPPV, Periodic Safety Reports We Are Your Partner for Success in Japan Get in touch