Sri Venkateswara Institute of Medical Sciences (SVIMS)

Established by AP State Legislature Act 1995 | Recognized under UGC 12(B)

Pharmacovigilance & Medical Device Adverse Event Monitoring Centre

Pharmacovigilance Committee | PvPI (Pharmacovigilance Programme of India) | MvPI (Materiovigilance Programme of India)

Adverse Drug Reaction Monitoring Centre (AMC)

SVIMS, Tirupati is recognized as an Adverse Drug Reaction Monitoring Centre (AMC) and approved by the Indian Pharmacopoeia Commission - National Coordinating Centre (PvPI), Ghaziabad on 08/07/2015. We play a crucial role in safeguarding patient health by systematically monitoring, assessing, and responding to adverse drug reactions (ADRs).

Objectives:

Key Activities:

Committee Members (PVC)

S. No Name of the Faculty Designation PVC Role
01Dr. Usha KalawatPrincipalChairman
02Dr. R. RamProfessor & HOD of NephrologyCo-Chairman
03Dr. K. Umamaheswara RaoProfessor & HOD of PharmacologyCo-ordinator
04Dr. C. PallaviAssociate Professor of PharmacologyDeputy Co-ordinator
05Dr. K. ChandraSekharAssistant Professor of MedicineMember
06Dr. Y. MutheeswaraiahProfessor & HOD of General SurgeryMember
07Dr. K. Vijaya Chandra ReddyProfessor of PharmacologyMember
08Dr. Punith PatakProfessor & HOD of PaediatricsMember
09Dr. A. SurekhaAssociate Professor & I/C HOD, DermatologyMember
10Mrs. PrabhavathiD.D. NursingMember
Junior Pharmacovigilance Associate: Mrs. M.K. Manisha, M. Pharm, appointed by the Indian Pharmacopoeia Commission- NCC (PvPI), Ghaziabad.

Medical Device Adverse Event Monitoring Centre

Officially designated as a Medical Device Adverse Event (MDAE) Monitoring Centre with effect from August 23, 2022. This initiative enhances patient safety by systematically monitoring events related to medical devices.

Our Commitment: At SVIMS, pharmacovigilance is a critical element of clinical care. We aim to minimize drug-related harm and continuously improve the standards of patient safety and public health.