Pharmacovigilance – Extended Program

Srinath k
Last Update October 30, 2022
0 already enrolled

About This Course

Pharmacovigilance – Extended Program

Guaranteed full Scholarship for Top 5 Student of the course to learn SAS Programming directly from SAS company!


Call Advisors

9381210106, 6296344286, 9032514145,

9032514147, 8125516279 , 9390838532


One Step Registration link:

1 Month training – 7pm to 8 pm, 8pm to 9pm

Oct – 31, Nov – 6, 7, 8, 9, 10, 11, 14, 15, 16, 17, 18, 21, 22, 23, 24, 25


Registration Details

Total Course Fee: 5,000 + 18% GST

Mode: Zoom or Zoho Webinar – Link will be emailed on 30th Oct 2022.


Course Objective

Extensive knowledge with detailed understanding of basics imparted to equip you to work at any global Clinical research organizations (CROs) or Pharmaceutical companies or Pharmacovigilance service providers.

Understand the topic to gain the skills, knowledge and competencies of a right candidate for the
Pharmacovigilance sector.

Overview of practical aspects of Pharmacovigilance activities as per the global standards like safety reporting, medical evaluation, casualty assessment, expectedness assessment, case processing, narrative writing, MedDRA etc. to make a student industry ready.

Learn to appear the interview with confidence and grab the best deserved job based on your skillset.


Why attend this training?
Pharmacovigilance & Clinical research is rapidly growing industry globally with growth rate of more than 40% per year. Being a particular specialty, this sector requires trained and skilled workforce, with basic understanding of Clinical Research, Clinical Data Management & pharmacovigilance. This is why, over any unskilled candidates, they prefer them who already understands the basics of safety reporting & it’s impact. In a typical pharmacovigilance department or specialized pharmacovigilance company, there are several positions. Pharmacovigilance offers excellent growth prospects. Here are some of the positions a fresher can get selected for- Drug Safety Associate; Drug Safety Scientist; Aggregate Report Scientist; Pharmacovigilance associate; Safety report specialist etc.


What are the benefits of this course after college?
At the end of this course you’ll gain comprehensive knowledge to the pharmacovigilance basics, clinical research processes, drug development process, regulatory affairs, essential documentation, roles and responsibilities, ethics, monitoring, conduct and management of trials, extensive training on Pharmacovigilance (PV) related issues. In other words, the students taking this course will completely industry ready as freshers.



Session 1: Introduction to Pharmacovigilance, history, background
Session 2: Introduction and Evolution of Pharmacovigilance Regulatory And International Agencies
Session 3: Signal Detection and Risk Management Agreegate safety reporting
Session 4: Adverse drug reactions, Individual Case Safety Report, Different types of safety reports
Session 5: Case processing overview (ICSR), Case Receving and Triaging, Labeling Assessment, Causality Assessment
Session 6: Understanding MedDRA and other drug dictionaries, Medical Coding, MeDRA Coding Conventions
Session 7: Narrative writing workshop
Session 8: Understanding workflow, growth and future aspects of PV industry
Session 9: Preparation for Pharmacovigilance interview
Session 10: Question & Answers session

Learning Objectives

This is in association with Indian Pharmacy Graduate Association.
This course benefits all the final year, recent graduate and working professionals.
Guaranteed Scholarship for Top 5 performers on SAS Programming Course

Target Audience

  • All medical and bio-science students and professionals.




Session 1: Introduction to Pharmacovigilance, history, background

Session 2: Significance of Pharmacovigilance, workflow of PV

Session 3: What is risk management & signal detection? What is patient safety? How PV helps in risk management & patient safety?

Session 4: What is MedDRA? History of MedDRA.

Session 5: Scope of MedDRA. What is the importance of MedDRA?

Session 6: Structure of MedDRA. How is MedDRA necessary in PV?

Session 7: Workflow of PV industry & career growth

Session 8: What are different types of reports and sources of the reports? What are different types of cases? What is case processing/ reviewing/ triaging/ medical review/submission

Session 9: Different aspects of PV interview, challenges and solutions.

Session 10: Question, Answers & doubt solving session

Write a review


All Levels
Duration 20 hours

Material Includes

  • All the materials are provided during training.
Select the fields to be shown. Others will be hidden. Drag and drop to rearrange the order.
  • Image
  • SKU
  • Rating
  • Price
  • Stock
  • Availability
  • Add to cart
  • Description
  • Content
  • Weight
  • Dimensions
  • Additional information
  • Attributes
  • Custom attributes
  • Custom fields
Click outside to hide the compare bar
Wishlist 0
Open wishlist page Continue shopping
Alert: You are not allowed to copy content or view source !!