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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