Our PV team is qualified and experienced in providing PV services in following areas:

  • Australian pharmacovigilance contact person 
  • Submitting serious adverse reaction reports to TGA
  • Notifying significant safety issues to TGA
  • Managing safety data exchange agreements
  • Literature search
  • Update product labels and product information with new safety information
  • RMP and ASA development
  • Reporting Quality defect issues, adulterated products, counterfeit products to TGA
  • Managing product recalls

Seed Pharma provides the Pharmacovigilance services like Literature monitoring, Adverse event reporting, QPPV, etc to meet regulation as per TGA.Seed Pharma has a Qualified Person for Pharmacovigilance(QPPV) who will be actively looking for requirements and assisting you to meet TGA requirements.