Pharmacovigilance Course

Pharmacovigilance is a sub field of Pharmacy which includes research, detection, assessment and analysing the drug’s safety or safety of medicinal products. It is a very popular course in Medical Science. This course is suitable for the candidates who wish to join any pharmaceutical industry or pursue research in the future.

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Pharmacovigilance Course

Here in this course GAADS will provide excellent material for pharmacovigilance and there is vdery important interview Questions and answers also. Don't miss the valuable material. Even rural background students also understand the language mentioned in this material. All the best.

Pharmacovigilance is a continuous process accepted for safety evaluation accompanied by steps to improve safe usage of medicines..

Pharmacovigilance is considered to be one of the best career option for life science and pharmacy graduates. It mainly deals with reporting and analysing of medicine side effects and ensure drugs in the market are safe and secured

The principal goal of pharmacovigilance is to influence safer usage of medicines. But, it faces increasing pressure to analyse more data sooner, monitor risks more broadly, and accurately report patient events globally.

Pharmacovigilance is regarded as a great career option for interested aspirants as it reflects a well-defined and growing career path. There is a faster career growth leading to managerial as well as director roles eventually along with a quite decent salary package. Here, in this article, we have highlighted different curriculum and career aspects of Pharmacovigilance. For someone willing to initiate his/her career in Pharmacovigilance, the entry-level job is that of a Drug Safety Associate (DSA). All DSAs get involved in developing various cases, checking for Minimum Safety Information (MSI), reconciliation and then following up processes, along with data entry of all information available in the document and medical coding.

Why GAADS Pharmacovigilance Course

Live sessions with
industry experts

Enhance Your
Writing skills


Doubt Clearing

Mock Interviews


Soft Skills Training

Full-fledged Course

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Course Objectives

    This Program would help you to gain in-depth knowledge on the best way to collect and report adverse events and safety data and manage the risk associated with and risk to pharmaceutical products. Its unique format will provide you with the key skills and knowledge needed to operate a fast, effective drug safety or pharmacovigilance program.

Eligibility Criteria for Pharmacovigilance

    For aspirants to undertake a professional career in Pharmacovigilance, the minimum eligibility conditions for applying for the course are as follows:
  • Graduate or postgraduate degree in pharmacy or life sciences with securing at least 50% marks in aggregate.
  • Graduate or postgraduate degree in Pharmacy or Pharmaceutical Sciences
  • Graduate or postgraduate degree in Medicine.

Required skillset for Pharmacovigilance:

    For any aspiring candidate to specialize and become DSS (Drug Safety Scientist), one needs to have the following skillset:
  • Knowledge of Medical coding
  • Narrative and Scientific writing
  • Good understanding of medical terms
  • Basic knowledge of regulatory affairs, ICH-GCP, and other compliances
  • An eye for detail
  • Ability to maintain meticulous records
  • Excellent analytical & problem-solving skills
  • Effective Communication
  • Systematic Approach to Tasks
  • Good interpretive skills
  • Basic level of English and good quality of internet connection, Desktop /Laptop/Smartphone required (Since dealing with online mode)
  • Basic Knowledge in Pharmaceutical/ medical field

What you'll learn

  • History and Evaluation of Pharmacovigilance & terminologies in Pharmacovigilance.
  • Drug discovery and development phases & Introduction to drug safety.
  • Types of adverse events & Pharmacovigilance global guidelines.
  • Medical dictionary for Regulatory activities(MedDRA)
  • Case fallow up, PV audits and inspection, Vaccine vigilance and materiovigilance


Module Basic

The evolution of clinical research is a long and fascinating journey. The history of clinical research accounts for the high ethical, scientific, and regulatory standards represented in current practice. In this module students will understand how it all began and evolve.

Regulatory medical writing is for clinical research document preparation. It is important for students to have the in-depth understanding of the various aspects of clinical research.

Good clinical practice (GCP) is an international ethical and scientific quality standard for designing, recording and reporting clinical trials that involve the participation of human subjects. It is important for students to understand the principals of GCP and its implementations. This module will help students to understand the various aspects of GCP in clinical research.

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Frequently Asked Questions

Pharmacovigilance is an excellent career choice for people interested in the medical industry and passionate about drug safety. and that resounding yes! The demand for pharmacovigilance professionals is expected to continue to rise in the coming years.
Future PV will require dedicated sub-functions with the sole responsibility of direct engagement with patients and patient groups through their preferred communication channels to collate questions and concerns and to more effectively translate safety-related information to the layperson.
The study of pharmacy or pharmaceutical science at the graduate or postgraduate level. Medicine at the graduate or postgraduate level.
Pharmacovigilance aims to preserve general health by identifying, evaluating, and minimizing health issues to ensure that the benefits of accessible treatments outweigh the potential risks.
Absolutely Pharmacovigilance because Pharmacovigilance is the best field to study about the available drugs as well as their side effects. Pharmacovigilance is completely research based stream and it is most demanding domain for pharmaceutical professionals.
It is a scientific discipline that involves reporting and assessing the side effects of a medicine. It is mainly due to the function of Pharmacovigilance professionals that the medicines in the marketplace that we consume are safe, and all those that are identified as hazardous are taken off the market.
The goal of safety monitoring in clinical trials is to identify, evaluate, minimize and appropriately manage risks. In Europe, Risk Management Plans (RMPs) are required by the EMA as part of the drug approval process.