Our PV team is qualified and experienced in providing PV services in following areas:
- Australian pharmacovigilance contact personÂ
- 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.