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Mohammad Rafi is a seasoned Pharmacovigilance professional with 13 years of experience in adverse event reporting, pharmacovigilance, and clinical research. He holds a Master of Pharmacy degree and is certified in various areas, including pharmacovigilance and clinical trials.

Credentials

  • Adverse Events Following Immunization
    World Health Organization
    Oct, 2019
    - Apr, 2026
  • Life Member
    Indian Pharmacological Society
    Mar, 2018
    - Apr, 2026
  • ORCID
    ORCID
    Jan, 2016
    - Apr, 2026
  • Certificate of Appreciation
    Indian Pharmacopoeia Commission by former DCG(I) Dr. G.N. Singh
    Aug, 2015
    - Apr, 2026
  • Fundamental of Clinical Trials
    Harvard University
    Feb, 2014
    - Apr, 2026
  • Take Your Medicine - The Impact of Drug Development
    The University of Texas System
    Dec, 2013
    - Apr, 2026
  • Vaccine Safety Basics
    World Health Organization
    Mar, 2013
    - Apr, 2026
  • Health in Numbers: Quantitative Methods in Clinical Public Health Research
    Harvard University
    Feb, 2013
    - Apr, 2026
  • VigiFlow Certification on ICSR processing
    Uppsala Monitoring Centre
    Dec, 2010
    - Apr, 2026
  • Pharmacist
    Madhya Pradesh State Pharmacy Council, Bhopal
    Jun, 2012
    - Apr, 2026
  • Fouth Asia Pacific Pharmacovigilance Training Course
    Uppsala Monitoring Centre
    Jan, 2018
    - Apr, 2026
  • 31st M.P. Young Scientist Fellowship
    Madhya Pradesh Council of Science & Technology, Bhopal
    Feb, 2016
    - Apr, 2026

Experience

    • India
    • Pharmaceutical Manufacturing
    • 300 - 400 Employee
    • Pharmacovigilance Associate
      • Jun 2016 - Present

      Quality review of ICSRs.SUSAR identification.Signal detection.Risk minimizationPublishing case reports and research articles

    • Technical Associate
      • Apr 2011 - May 2016

      Seriousness & causality assessment of ICSRs.Referring safety database for unlisted & unlabelled terms e.g. Vigibase, FAERS, SmPC, PIL, CCDS, RSI, etc. ICSRs case processing using MedDRA & WHO-DD coding.Adhering to SOPs, EMA guidelines & GVP modules

    • Technical Associate
      • Nov 2010 - Mar 2011
      • Indore, Madhya Pradesh, India

      Established Pharmacovigilance dept. and culture of ADR reporting at hospital associated with medical college-pan India (PvPI).ADR monitoring, collection, assessment and processing using WHO-UMC's VigiFlow network.Counseling patients to minimize ADRs.Coordinating with clinicians in identifying the suspected drugs causing ADRs and related queries.Archiving local database of ADRs.

  • Novartis India
    • Hyderabad, Telangana, India
    • Intern - Drug Safety & Epidemiology, PV Operations
      • Jan 2010 - Mar 2010
      • Hyderabad, Telangana, India

      ARGUS 8.0 safety case processing.Triaging ICSRs.Duplicate search for ICSRs.Entering follow up information.Archiving CIOMS & Medwatch forms.Reporting to Group head. Communication with stakeholders.

Education

  • 2008 - 2010
    NIMS Institute of Pharmacy, NIMS University, Jaipur
    Master of Pharmacy, Pharmacovigilance
  • 2004 - 2008
    Institute Of Pharmacy, Vikram University Ujjain
    Bachelor of Pharmacy (B.Pharm.), Pharmaceutical Sciences
  • 2001 - 2003
    Sanmati Higher Secondary School - India
    Higher Secondary (10+2)
  • 2000 - 2001
    Bright High School, Indore
    High School
  • 1998 - 1999
    Indian Community School, Benghazi, LIBYA (North Africa)
    Class 8th to 9th, CBSE
  • 1996 - 1997
    Asian Community School, Al-Marj, LIBYA (North Africa)
    Class 6th to 7th
  • 1993 - 1995
    Bright high school indore

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Industry Focus. “Pharmaceutical Manufacturing”

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