Pharmacovigilance and Drug Safety Management

Mentor Based

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Duration

10 weeks (may vary by course provider).

Eligibility

Mode

Online, with video lectures, reading materials, quizzes, and group discussions.

Course Aim

The aim of this course is to equip participants with a comprehensive understanding of pharmacovigilance principles, processes, and best practices. It focuses on the safe monitoring and reporting of adverse drug reactions, compliance with regulatory requirements, and ensuring the overall safety of pharmaceutical products.

Course Objectives

• By the end of the course, participants should be able to:
• Understand the fundamental concepts and significance of pharmacovigilance.
• Identify and report adverse events and adverse drug reactions accurately and efficiently.
• Analyze safety data to assess the benefit-risk profile of pharmaceutical products.
• Comprehend global pharmacovigilance regulations and guidelines.
• Develop and implement risk minimization strategies.
• Prepare and submit regulatory reports in compliance with regulatory authorities.
• Collaborate effectively with cross-functional teams in the pharmaceutical industry.
• Stay informed about emerging trends and challenges in pharmacovigilance.

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Program Structure

The course will cover a range of modules (subject to change based on the course provider), including:
• Introduction to Pharmacovigilance
• Adverse Event Detection, Collection, and Reporting
• Signal Detection and Management
• Benefit-Risk Assessment
• Regulatory Requirements and Compliance
• Risk Minimization and Risk Communication
• Pharmacovigilance in Clinical Trials
• Safety Data Analysis
• Pharmacovigilance Auditing and Inspections
• Emerging Trends and Future Challenges




What You Will Get?

Program work is completed through online system under the guidance of program coordinator.

e-LMS for smarter Learning

24 x 7 open chat box

Excellent option for summer project

Online live lectures from the experts

Prepare real time projects

Certificate on project completion

Various Job Opportunities

This course is intended for professionals and individuals interested in pharmacovigilance and drug safety, including:
• Pharmacovigilance professionals and practitioners
• Regulatory affairs specialists
• Clinical research and development personnel
• Healthcare practitioners
• Quality assurance professionals
• Graduates seeking a career in pharmacovigilance

Steps For Enrollment

Step 1: Click On The Below Mentioned Link “Apply Here”
Step 2: Fill All Basic Details Of Yours (Name, Email Id, Contact Details, Image)
Step 3: Choose Your Program, Session And Duration Of Program
Step 4: Fill Payment Details In The Form And Submit
Step 5: Hurray! You Will Get Your Login Credential Within 48 Hrs.

Skills to Score

Fee Plan

Basic Course

3 Month Mentor Based Course

INR 12,999/- or USD 199

  • Access to e-LMS
  • Immediate commencement
  • Study material at your doorstep
  • Project Guidance from Subject Experts
  • Paper Publication Opportunity
  • Self Assessment
  • Final Examination
  • Printed certification
  • Printed Marksheet

Advanced Course

6 Month Mentor Based Course

INR 22,999/- or USD 349

  • Access to e-LMS
  • Immediate commencement
  • Study material at your doorstepv Complete Basic Course
  • Complementary Scientific Technical Writing
  • Real Time Project for Dissertation
  • Project Guidance from Subject Experts
  • Paper Publication Opportunity
  • Self Assessment
  • Final Examination
  • Printed certification
  • Printed Marksheet

Course Outcomes

• Upon completing this course, participants are expected to:
• Possess a strong foundation in pharmacovigilance principles and practices.
• Be proficient in identifying, documenting, and reporting adverse events and reactions.
• Demonstrate the ability to assess benefit-risk profiles of pharmaceutical products.
• Understand and apply global pharmacovigilance regulations.
• Develop and implement effective risk minimization strategies.
• Prepare accurate regulatory reports and documentation.
• Collaborate seamlessly with teams in the pharmaceutical industry.
• Stay informed about evolving trends and challenges in pharmacovigilance.

Join Now!

It’s time for you to be enhance your knowledge and be an edge above others. Register yourself and get started today.

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