Description
Drug safety teams ensure adverse events are collected, assessed, and reported within strict timelines. This course introduces case processing, MedDRA, and the collaboration between PV and clinical teams.
You will practise writing concise narratives and thinking in terms of causality and expectedness.
Program highlights
Case lifecycle
Follow a case from report to submission-ready record.
Medical writing in PV
Narrative structure and clarity under time pressure.
Signal awareness
Understand how aggregate reviews connect to safety science.
Career path
Entry roles in case processing and medical review support.
Eligibility
This program is designed for pharmacy and life-science graduates targeting roles in pharma, CROs, and healthcare evidence teams.
- B.Pharm, M.Pharm, Pharm.D
- M.Sc / B.Sc (Life Sciences — Biotechnology, Microbiology, Biochemistry, etc.)
- B.E. / B.Tech / M.Tech (Biotech / Biomedical Engineering or related)
- BDS, BAMS, BHMS, MBBS, BPT, Nursing — contact us for pathway advice
- Other graduates — we will confirm fit for your target role
Course syllabus
Outline reflects core topics; live batches may adjust emphasis based on cohort profile and industry updates.
- PV workflows: intake, triage, follow-up, and reporting
- MedDRA basics and medical concept handling
- Regulatory reporting timelines (introductory level)
- Literature screening hooks and documentation
Key features
Live instruction
Structured live sessions with Q&A and real-world examples.
Practice & assignments
Exercises aligned to what employers ask in screening and interviews.
Mock interviews
1 mock interview included in the program design.
Mock tests
2 mock tests to reinforce concepts under time pressure.
Learning platform
Through our learning workflow, students get access to session materials, recordings (where applicable), assignments, and revision notes. Instructors share batch-wise instructions for submissions and assessments so you can learn in a structured way alongside your live classes.
Fees
Enquire for batch-wise fees. Fee structure can vary by batch format (online vs offline) and promotions — our team will confirm the exact amount and payment steps when you enquire.
Enquire nowAdmission process
Raise an enquiry
Use our website, email, or WhatsApp to share your profile and program interest.
Speak to a program advisor
We confirm eligibility, batch timing, and fee structure for your chosen track.
Apply & register
Select your program, complete the application, and pay the registration fee as advised.
Application review
We acknowledge your enrolment and share access / class schedule details.
Start learning
Join live sessions, complete assignments, and access placement support milestones.
Certification
On successful completion of the program requirements, CliniWings awards a participation / completion certificate for the enrolled track. External vendor or international board exams (where relevant to your career goal) are separate and optional.
Placement support
Our placement process focuses on employability: CV refinement, mock interviews, and guidance on how hiring works in pharma and CROs. We do not guarantee jobs, interviews, or internships. Outcomes depend on market conditions, role fit, and individual performance.
For more detail, read our placement-related communication on the Placements page and ask us directly if you need clarity.
Career opportunities
Skills from this program align with entry and early-career paths that value the following competencies:
- PV workflows: intake, triage, follow-up, and reporting
- MedDRA basics and medical concept handling
- Regulatory reporting timelines (introductory level)
- Literature screening hooks and documentation
Specific job titles vary by company; we help you map your profile to realistic role families during counselling.