Registration, tasks, submissions and human review are free. The verified certificate is optional: ₹99 after required approvals, subject to program dates.
Practise safety documentation without treating it as clinical advice
Pharmacy students and beginners exploring drug-safety terminology can use these fictional case exercises to practise careful documentation. Start by distinguishing a reported event, a suspected reaction and the evidence available in a case. Read the task's definitions before making a causality or severity classification; uncertainty belongs in the answer.
Your ADR, ICSR, RMP and PSMF exercises should preserve the fictional case label, explain the selected evidence and avoid inventing missing clinical facts. These are educational submissions, not regulatory reports or a qualification to perform professional drug-safety work. Compare healthcare/pharmacy analytics for dataset-oriented practice. Check the college requirements guide before assuming a pharmacy department accepts this format.
Your safety-documentation roadmap
The standard program assigns the seven briefs below plus a public LinkedIn offer-letter acceptance post. The starter assigns that onboarding post and the first two briefs. The dashboard contains the current submission instructions.
1. ADR Identification Basics
Read symptoms, medication history and event timelines to identify possible adverse drug reactions. Separate the recorded facts from your assumptions; a suspected relationship is not established causation.
Deliverable: A PDF report or document containing the case analysis and identified ADR table.
2. ADR Reporting & Documentation
Complete a structured reporting form from the supplied case. Preserve the distinction between unknown information and a negative finding; do not invent a dose, date or outcome to fill a blank.
Deliverable: A completed ADR reporting form as a PDF or accessible Drive link.
3. Causality Assessment
Use the brief's Naranjo or WHO-UMC approach to explain the relationship between a medicine and event. Show how the available evidence supports each judgment and where information is missing.
Deliverable: A Naranjo scoring worksheet and causality justification PDF.
4. Severity & Case Classification
Assess seriousness and expectedness using the supplied scenarios and references. Explain the case-level rationale instead of relying on a symptom label alone.
Deliverable: A serious versus non-serious case assessment PDF.
5. Individual Case Safety Report (ICSR)
Bring the case information together into a coherent narrative and the terminology mapping requested by the brief. Keep chronology, suspect products and assessment reasoning consistent across sections.
Deliverable: A completed ICSR narrative PDF.
6. Risk Management Plan (RMP)
Prepare an educational overview of the supplied safety profile, proposed pharmacovigilance activities and risk-minimisation measures. Explain how each proposed activity addresses the stated risk or information gap.
Deliverable: An RMP executive overview PDF.
7. Final PSMF Summary
Summarise the fictional organisation's oversight and safety-system arrangements using the pack's material. Treat the result as a learning document, not a production master file.
Deliverable: A PSMF summary PDF or accessible document link.
These cases are educational, not clinical
Every supplied patient and safety case is fictional. Do not use the material for treatment decisions, regulatory reporting or real product-risk conclusions. Reporting frequency alone does not prove causation. Do not upload real patient records or confidential safety reports in a public submission.
For a useful portfolio, include the fictional source reference, your method, unresolved information and limitations. Make your submission readable without a login. Review feedback may require a corrected assessment or more accessible proof.
Program dates and optional certificate
Choose 30, 45 or 60 days for the standard roadmap, or the three-task 7 Days Starter Instant Internship. The starter has no submission deadline while unpaid; its verified optional payment date becomes the end date after all three approvals. Standard access follows the dashboard's schedule and any explicitly confirmed instant option.
Workora does not promise a clinical qualification, government accreditation, stipend, job or college credit. Confirm acceptance with your college before enrolling for an academic requirement.
Register for Pharmacovigilance
Read the full fee and program explanation · Prepare your portfolio