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Live Industrial Program

Certificate Course in Pharmacovigilance

Ensuring Drug Safety and Compliance Through Expert Training

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MODE
Online/ e-LMS

TYPE
Mentor Based

LEVEL
Moderate

DURATION
3 Months

About

The Certificate Course in Pharmacovigilance offers an in-depth exploration into the critical role of drug safety monitoring in the healthcare industry. Throughout this month-long program, participants will engage with the fundamental concepts of pharmacovigilance, including adverse event reporting, risk management, and data analysis. The course is designed to blend theoretical knowledge with practical skills through case studies, regulatory document reviews, and real-world data evaluation exercises.

Aim

This program aims to provide comprehensive training in pharmacovigilance principles and practices, focusing on the monitoring, assessment, and prevention of adverse effects associated with pharmaceutical products. Participants will learn to ensure drug safety and compliance with global regulatory standards, enhancing patient care and public health outcomes

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Program Objectives

Develop a robust understanding of pharmacovigilance systems and their importance in healthcare.
Learn to effectively manage and report adverse drug reactions.
Understand global regulatory requirements and how to comply with them.
Analyze real-world evidence and case reports to improve drug safety.
Enhance skills in communication and collaboration with regulatory bodie

Program Structure

Key principles and methodologies of pharmacovigilance
Techniques for detecting, assessing, understanding, and preventing adverse effects
The regulatory environment and its impact on pharmacovigilance practices
Tools for data management and analysis in drug safety
Strategies for effective risk communication and management

Participant’s Eligibility

Undergraduate degree in Pharmacy, Nursing, Medicine, or Life Sciences.
Healthcare professionals involved in drug safety and patient care.
Individuals interested in a career in pharmaceutical regulation and public health.

Program Outcomes

Expert knowledge of pharmacovigilance protocols and practices
Ability to navigate and comply with international drug safety regulations
Proficiency in adverse event reporting and risk assessment
Skills in data analysis and interpretation for drug safety
Collaboration and communication skills with regulatory authorities

Fee Structure

Standard Fee: INR ~~49,998~~ USD ~~1,300~~

Discounted Fee: INR 24999 USD 650

We are excited to announce that we now accept payments in over 20 global currencies, in addition to USD. Check out our list to see if your preferred currency is supported. Enjoy the convenience and flexibility of paying in your local currency!

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Certificate

Program Assessment

Certification to this program will be based on the evaluation of following assignment (s)/ examinations:

Exam	Weightage
Mid Term Assignments	50 %
Project Report Submission (Includes Mandatory Paper Publication)	50 %

To study the printed/online course material, submit and clear, the mid term assignments, project work/research study (in completion of project work/research study, a final report must be submitted) and the online examination, you are allotted a 1-month period. You will be awarded a certificate, only after successful completion/ and clearance of all the aforesaid assignment(s) and examinations.