Certification training in Pharmacovigilance

Duration : 1.5 months

Overview

Pharmacovigilance plays a critical role in ensuring the safety and efficacy of drugs by monitoring, detecting, and assessing adverse drug reactions (ADRs). This Certification Training in Pharmacovigilance equips learners with the knowledge and skills to excel in this essential field. Designed for aspiring professionals and those seeking to advance their careers, the program provides in-depth insights into global PV processes, regulations, and practices.

Mode of training : Online and offline

Career opportunities

Pharmacovigilance Specialist

Drug Safety Scientist

Safety Data Analyst

Adverse Drug Reaction (ADR) Reporter

Comprehensive Curriculum

Covers all aspects of pharmacovigilance, from ADR reporting to global regulations.

Hands-On Training

Practical exposure to PV tools and systems for real-world application.

Industry-Expert Faculty

Learn from experienced professionals in pharmacovigilance and drug safety.

Placement Support

Resume building, interview preparation, and job assistance in leading pharmaceutical companies.

Learning Objective

History of Pharmacovigilance

Trace the evolution of pharmacovigilance and its significance in the healthcare system.

Process of PV

Understand the end-to-end pharmacovigilance workflow, from ADR reporting to risk assessment.

Pharmacovigilance Terminologies

Familiarize yourself with key PV terms and concepts essential for the field.

Good Vigilance Practice (GVP)

Learn the principles and standards outlined in GVP to ensure compliance and quality.

Narrative Writing

Master the art of creating clear and concise narratives for adverse event (AE) reports.

Pharmacovigilance Definitions

Gain a clear understanding of core definitions and their applications in real-world scenarios.

A.E. Reporting

Learn the critical steps for identifying, reporting, and managing adverse events effectively.

Pharmacovigilance in General

Develop a holistic view of PV, including its role in healthcare and drug development.

Pharmacovigilance Process

Detailed explanation of the PV process, including signal detection, risk assessment, and benefit-risk evaluation.

Global Regulations and Compliance

Study the regulations and guidelines of regulatory authorities like FDA, EMA, and WHO.

Eligibility

The minimum eligibility criteria for Certification Training in Pharmacovigilance would include either of the following:

Any degree in Bioscience/Life Sciences such as Biochemistry, Microbiology, Genetics, Biotechnology, Botany, Zoology etc

Any degree in Medicine such as MBBS, BDS, BPT, BAMS, BHMS, BUMS etc

Any degree in Pharmacy / Pharmaceutical Sciences

Any degree in Chemistry / Biostatistics / Bioinformatics

Any degree in Nursing / Allied Health

Students in their final year of graduation for the above courses are also eligible to apply

Candidates without any science background or candidates with some work experience in the clinical research / pharmaceutical industry / allied areas may also be eligible for this program. Please check with our counsellors for more information.

Academic Support

Towards the end of the program you will be provided placement assistance and career development support via our dedicate team working on placements.

In addition, each participant registered in the course is provided with a mentor who is an experienced industry professional. The mentor can be contacted at any time via email or phone.

Master Clinical Research & Get Your PG Diploma

Your fast-track to a global career in Clinical Trials.

Flexible Duration: Complete your specialized training with intensive, hands-on industry projects.
Industry-Aligned Curriculum: Master core modules designed by experts to meet global regulatory standards.
Global Recognition: Earn an ISO 9001:2015 Verified credential, instantly shareable on LinkedIn to boost your profile.
Career Success: Access our 100% Placement Support network with top CROs and leading Pharma companies.