WorkshopCompleted

How This 2-Day Workshop Changed My Perspective | Student Testimonial

Name: How This 2-Day Workshop Changed My Perspective | Student Testimonial
Start: 2026-06-09T07:51:00.000Z
Location: Oxford College of Engineering

The 2-Day Integrated Clinical Research & Pharmacovigilance Workshop conducted by Bangalore Clinical Research Institute (BCRI) at Oxford College of Engineering was designed to provide participants with a strong foundation in the clinical research industry through practical, industry-oriented learning. On Day 1, the workshop introduced students to Clinical Data Management (CDM), covering core concepts, data handling processes, and hands-on training using the Clinevo Safety Database. This practical exposure helped participants understand how clinical data is managed and maintained in real-world research environments. On Day 2, the focus shifted to Pharmacovigilance (PV), where students learned about drug safety monitoring, adverse event reporting, case processing, regulatory guidelines, and the critical role of pharmacovigilance in ensuring patient safety and healthcare quality. Through expert-led sessions, practical demonstrations, and interactive learning, the workshop equipped participants with valuable industry insights and foundational knowledge, helping them better understand career opportunities in Clinical Research, Clinical Data Management, and Pharmacovigilance.

Key Topics Covered

Data Entry
Data Validation
SAE Reconciliation
Medical Coding
Vendor Reconciliation
Data management Plan
PV
ISCR
Signal Detection
Aggregate Reporting
Narrative Writing
UMC

Hear from Shreya, a Biotechnology student, as she reflects on her learning experience from the 2-Day Integrated Clinical Research & Pharmacovigilance Workshop organized at Oxford College of Engineering. Shreya explains how the workshop offered a clear and practical overview of the clinical research domain. Day one introduced her to Clinical Data Management, where concepts were strengthened through practical sessions on the Clinevo Safety Database, giving her exposure to real-world data processes used in the industry. On day two, the focus moved to Pharmacovigilance, helping her understand drug safety responsibilities, case reporting, and regulatory importance, and how these processes contribute to patient safety and quality healthcare. ✨ An engaging and insightful program that adds strong value to a biotechnology student’s career journey.

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