Certificate Course in Pharmacovigilance (Online)

 

Features

  • 6 months Online course 
  • Industry oriented syllabus
  • Training of software in industry
  • Learn documentation in Pharmacovigilance including Narratives, RMP, PSUR and many more
  • This is same course available at locations such as Nashik, Pune and Satara. 
  • No placements are provided for this course. We only provide you placement assistance by emailing you job opportunities.

Certificate Course in Pharmacovigilance

₹30,000.00 Regular Price
₹15,000.00Sale Price
  • Eligibility

    • HSC Science Passouts
    • B. Pharmacy Students
    • M. Pharmacy Students
    • MSc / BSc Professionals or Students
    • Doctors (MBBS / BHMS / BAMS, etc) can also apply
    • Experienced Professionals

     

    Benefits along with course

    • Student helpline on 9696097866
    • Dedicated student coordinator to solve your queries online on WhatsApp or Skype
    • Virtual Learning Environment (VLE) e-learning portal
    • Android / iOS Application for learning
    • Scientific meetings updates – Get update on workshops and meetings directly on your mailbox.
    • Coverage of regulatory and government policies- Get updates on these via electronic information resource.
    • FREE Publication in Sci Journo – InClinition’s Science Journal
    • Access to Alumni Portal – InClinition Alma Connect

     

    Course Contents:

    1. Introduction and objectives of Pharmacovigilance
    2. Adverse drug reactions and their types: The difference between adverse drug reactions and adverse events
    3. ADR and Drug Dictionaries
    4. Signal detection, strengthening and analysis
    5. Safety databases – argus and arisg
    6. Good Pharmacovigilance Practices
    7. Pharmacovigilance methods and Electronic reporting E2b
    8. Safety data exchange agreements
    9. Sources of safety data- handling of reports from psp, clinical trials
    10. Literature surveillance – global and local
    11. Reference safety information and Xevmpd updates
    12. Pharmacovigilance regulations
    13. Reporting obligation for MAH and timelines for reporting
    14. Documentation in Pharmacovigilance (Aggregate reports.: Pader, psur, rmp, pbrer )
    15. Case Studies in Pharmacovigilance
    16. Setting Pharmacovigilance Centre
    17. Pharmacovigilance Programmes across globe
    18. Risk benefit assessment
    19. Resume writing
    20. Interview skills

     

     

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