Pharmacovigilance Course

Course Timeline

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.

$ 300

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This course includes:

Modules 14
Access Laptop and Mobile
Certificate of Completion Yes
Course Duration 2-3 Months

FAQs

Why GAADS Pharmacovigilance Course

Live sessions with
industry experts

Enhance Your
Writing skills

Resume
Building

Doubt Clearing
Sessions

Mock Interviews

Placement
assistance

Soft Skills Training
Session

Full-fledged Course
Structure

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

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:

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

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Testimonial

I was looking for an opportunity to learn more about medical writing before starting my career in clinical research. The training helped me to understand medical writing from the grass-root level leading me to perform various activities efficiently within a short time span. The training starts with basic learning and gradually shifted to advance learning as per my comfort and capability.

Parul Manocha

IP University Student

It was a great experience for me and yes I have gained a lot of knowledge like protocol writing, safety narrative writing, CSR & interview skills and how this course and training plays a vital role in career growth. So the aggregate is that it really matters what I gained from this training program.

Parul Vashista

Delhi University

This training has helped me to build up my skills which I was not even aware off. I am really grateful that I enrolled for this training. I am thankful to you for being our mentor and guiding us at every step in this training.

Rani Sana

Delhi University

I am Mahaprasad from Xavier University want to state that, it was a wonderful experience for me to get training, it was a privilege for me that you were my mentor, throughout the session who guided and supported me a lot. And once again thank you so much.

Mahaprasad

Xavier University Bhubaneswar

Thank you, you are inspiration for us, your knowledge, experience and behaviour are amazing, we learnt a lot from this training.

Yograj Thakur

IP University Student

Module Basic

Module 01

Historical Evolution of Clinical Research Regulations

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.

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Pharmacovigilance Course

Course Timeline