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.

We offer:

  • 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.

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