PvPI-Adverse Drug Reaction Monitoring Centre (AMC)

Scope / Objectives :

  • To monitor the ADR
  • To optimize safe and effective use of medicines in our set up
  • To create awareness amongst health care professionals about the importance of ADR reporting
  • To monitor benefit-risk profile of medicines
  • Generate independent, evidence based recommendations on the safety of medicines
  • Support the CDSCO for formulating safety related regulatory decisions for medicines
  • Communicate findings with all key stakeholders
  • Create a national centre of excellence as par with global drug safety monitoring standards

SUSPECTED ADVERSE DRUG REACTION REPORTING FORM – click here

 

Recognition as Medical Device Adverse Event Monitoring Centre(MDMC) under the Materiovigilance Programme of India (MvPI)-Reg. Recognition of your Institute as Adverse Drug Reactions Monitoring Centre(AMC) under PvPI.