Pharmaleaf has the expertise and resources to hold licenses on behalf of overseas clients / sponsors. The safety of our products and the health and well-being of our patients are our highest priority.
Pharmaleaf have its own Pharmacovigilance (PV) cell which will be monitored by qualified medical practitioners on regular basis.
- Safety monitoring (Collection and processing AEs / ADRs) of the products (for which Pharmaleaf holds the manufacturing licenses as well as import licenses).
- Handling of PV activities in compliance with Indian regulatory guidelines (NCC-PvPi, CDSCO).
- Periodic benefit and risk assessments with appropriate Risk management plans.
If you would like to report an adverse event involving our products, please download and fill the appropriate ADR form (see link below) and mail our Pharmacovigilance team at firstname.lastname@example.org. Please ensure to attach the completed ADR form in the mail.