Advanced Program in Pharmacovigilance

Pharmacovigilance is the pharmacological science related to the detection, assessment, understanding and prevention of adverse effects.



What will I learn?
  • Drug Safety Associate role
  • Safety Processing Expert role
  • Clinical Research Scientist role


Curriculum for this course
10 Lessons
Introduction to Pharmacovigilance
1 Lessons
Pharmacovigilance Overview
1 Lessons
Introduction to Adverse Events
1 Lessons
Regulatory guidelines and laws
1 Lessons
Adverse Event Reporting System
1 Lessons
PVPI
1 Lessons
Individual Case Safety Report (ICSR)
1 Lessons
Narrative Writing
1 Lessons
Coding with MedDRA
1 Lessons
Expedited reporting and PSUR
1 Lessons
Requirements
  • B.Pharm, M.Pharm and Pharm.D
  • B.Sc and M.Sc Life Sciences
  • BAMS, BHMS, BDS and MBBS
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Description
Pharmacovigilance is the science of collecting, monitoring, researching, assessing and evaluating information from healthcare providers and patients on the adverse effects of medications, biological products, herbalism and traditional medicines with a view to: identify new information about hazards associated with medicines preventing harms to patients. Pharmacovigilance is particularly concerned with adverse drug reactions, or ADRs, which are officially described as: “A response to a drug which is noxious and unintended, and which occurs at doses normally use for the prophylaxis, diagnosis or therapy of disease, or for the modification of physiological function.

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About the instructor
clinical research clincal trails
  • 10 Reviews
  • 45 Students
  • 10 Courses
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Clinical Research Program Trainer
Clinical Research Program Trainer
Student Feedback
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Reviews
  • Mon, 25-Feb-2019
    Best online course content for CR professionals.
  • Sat, 27-Apr-2019
    Sreeraj T
₹13500
Includes:
  • 10 Lessons
  • Four Month Access
  • Self Paced Learning
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