Healthcare and Clinical
Pharmacovigilance
Understand drug safety monitoring, adverse event reporting and the regulations behind them.
Who it’s for
Pharmacy and life sciences learners interested in drug safety.
Listed under these streams. We confirm any prerequisites with you before you register.
What you’ll study
- 01Drug safety fundamentals
- 02Adverse event case processing
- 03MedDRA coding overview
- 04Signal detection basics
- 05Regulatory reporting
- 06Safety databases
The full session-by-session plan is in the domain brochure. Ask admissions and we will send it to you.
What you’ll build
Practice tasks
Short assignments after each block of sessions, from the first week onwards. Each one is reviewed, so you know exactly what to improve.
Your domain project
In weeks six and seven you take on a project that pulls the whole curriculum together. Briefs are set for each batch.
How it runs
- Duration
- Two months (8 weeks)
- Program fee
- ₹9,999₹14,999
- Learning platform
- Sloka Academy LMS, hosted on Teachmint
- Completion
- Certificate on meeting the program requirements
Batch dates, class timings and the internship arrangement for Pharmacovigilance are shared by admissions when you get in touch.
Where it can lead
- Drug Safety Associate (Trainee)
- Pharmacovigilance Associate
- Case Processing Associate
Examples of roles this domain relates to. The program does not guarantee a job or placement.
Related
More in Healthcare and Clinical
Ready for Pharmacovigilance?
Call or email admissions. We will confirm the next batch date, check the fit with your background and explain how pre-registration works.