Ravindra Kumar Verma
Pharmacovigilance Lead, Quality & Compliance, Medical Writing, Safety Labeling, SERM
- Role
- Pv Specialist India & Em Deputy Pvoic (India), Deputy Qppv (Em) at Dr. Reddy's Laboratories
- Location
- Hyderabad, TG, IN
- LinkedIn followers
- 500 followers
About Ravindra Kumar Verma
Detail-oriented, methodical, goal-driven and self-motivated drug safety expert offering over 15+years of experience in Pharmaceutical industry. Specialties: Adverse Drug Reaction Data Base (ARISg), ARGUSProduct Guidance DocumentsPeriodic Safety Update reports (PSURs)United States Periodic Reports (USPRs)Safety NarrativesInvestigator\'s BrochureClinical Study ReportsClinical Overview (PAD CO CTD)Pharma Web Synopsis (PWS)
Experience
Pv Specialist India & Em Deputy Pvoic (India), Deputy Qppv (Em)
Jan 2026 — Present · Hyderabad, IN
Pharmacovigilance professional supporting the oversight and maintenance of the PV system for India and Emerging Markets. In my role as Deputy PVOIC (India) and Deputy QPPV (EM), I act as a key PV contact for Emerging Markets and work closely with cross‑functional teams to ensure regulatory compliance and high-quality safety operations.My experience includes oversight of case intake and quality, safety query management, implementation of SDEAs, reconciliation activities, deviation and CAPA management, SOP support, and delivery of PV training. I am committed to maintaining strong compliance with country-specific regulations and internal quality standards.
Education
Hamdard University, New Delhi
B.Pharma, Pharmacy
2003 — 2007
Hamdard University, New Delhi
Post Graduate Diploma in Regulatory Affairs, DRA
2009 — 2010
Hamdard University, New Delhi
M. Pharma, Pharmacology
2007 — 2009
Lucknow Christian Degree College
BSc, Zoology
1998 — 2001
Skills
- Medical Writing
- Clinical Study Design
- Ich-Gcp
- Clinical Trials
- Sop
- Drug Safety
- Medical Affairs
- Oncology
- Pharmacovigilance
- Pharmacology
- Meddra
- Clinical Research
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