Course Description

The Certificate in Pharmacovigilance is a 2-month specialized online program that focuses on the principles and practices of drug safety monitoring and adverse event reporting. Designed for students and professionals from pharmacy, life sciences, and healthcare backgrounds, this course provides a detailed understanding of how medicines are monitored for safety once they reach the market.

The curriculum emphasizes both the scientific and regulatory aspects of Pharmacovigilance, including signal detection, case processing, data analysis, and risk assessment. Through interactive sessions and real-world examples, learners gain the expertise needed to contribute effectively to global drug safety operations and regulatory compliance.

What You’ll Learn From This Course

• Core concepts of Pharmacovigilance and drug safety monitoring systems.
• Understanding of adverse event (AE) reporting, signal detection, and risk management.
• Familiarity with global regulations such as ICH, WHO, FDA, and EMA guidelines.
• Overview of case processing workflows and safety database management.
• Practical knowledge to support roles in pharma companies, CROs, and regulatory agencies.

Certification

After successful completion, participants will be awarded a Certificate in Pharmacovigilance from NexVed Clinical Research Academy. This certification validates your understanding of drug safety science and qualifies you for roles such as Pharmacovigilance Officer, Drug Safety Associate, Case Processor, or Medical Reviewer.

The course enhances employability in the pharmaceutical, biotechnology, and healthcare sectors, empowering learners to build a rewarding career in ensuring the safety and efficacy of medicinal products worldwide.