Pharmacovigilance plays a vital role in ensuring the safety of pharmaceutical products throughout their lifecycle. This course is designed to equip learners with practical, job-ready knowledge that reflects real-world industry practices. You will gain hands-on experience in adverse event reporting, database handling, regulatory submissions, and risk management planning.
The training also includes modules on signal detection, literature screening, audit preparation, and medical writing. With expert-led sessions and simulated tasks, learners will build a strong foundation in PV operations. The course concludes with CV and LinkedIn optimisation to boost career readiness for roles such as Drug Safety Associate, Pharmacovigilance Reviewer, or QPPV.
Curriculum
- 10 Sections
- 0 Lessons
- 10 Weeks
- Module 1 Introduction to Pharmacovigilance0
- Module 2 Adverse Event Reporting 0
- Module 3 PV Database and Tools0
- Module 4 Signal Detection Risk Management0
- Module 5 Risk Management0
- Module 6 PBRERs and DSURs 0
- Module 7 Literature Screening & Medical Writing0
- Module 8 Safety Section of the CSR0
- Module 9 Audits, Inspections & Compliance0
- Module 10 CV and Linkedin Optimisation for Career Pathways 0
Kwabena
Victor Maduka
I would like to undergo this training, but my query is, will there be real practical section in the laboratory of will it end in virtual demonstrations only?
pharmalinkacademy
Hi Victor, yes this course includes alot of practical work. This is not lab based, rather real world projects you would be assigned to in your career within PV