Pharma To Market can assist you with meeting your Pharmacovigilance requirements throughout Asia Pacific through our effective systems assuring local safety responsibility of your products on the market.
Safety data exchange agreements
ICSR management, including collection, evaluation, processing, distribution and reporting
Act as a QPPV (Qualified Person Responsible for Pharmacovigilance)
Preparation of PSURs
Literature screening and review
Preparation of Risk Management Plans (RMP)
Preparation of Australian Specific Annex or Singapore Specific Annex x to complement your existing EU/US RMP
Preparation of Risk Management Plan (RMP) waivers
Contact us to discuss your Pharmacovigilance needs.