Meet your Pharmacovigilance requirements

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

Preparation of PSURs

Literature screening and review

Preparation of Risk Management Plans (RMP)

Preparation of Risk Management Plan (RMP) waivers

Act as a QPPV (Qualified Person Responsible for Pharmacovigilance)

Preparation of Australian Specific Annex or Singapore Specific Annex to complement your existing EU/US RMP

ICSR management, including collection, evaluation, processing, distribution and reporting

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