he Future of Integrated Safety Monitoring
As safe drugs and medical devices begin with robust risk management and vigilant monitoring
Workshop Highlights / Topics Covered
✔️ How to identify , prevent and minimize the harm caused by medicines and medical devices to ensure patient safety and public health
✔️ Indian regulatory framework: CDSCO, MDR 2017, PvPI & MvPI
✔️ Practical guidance on adverse event reporting, timelines, and documentation
✔️ MedDRA / IMDRF coding aligned with ISO 14971:2019 – Risk Management
✔️ Detection , Risk assessment & Post -Market Surveillance , best practices
✔️Introduction to Pharmacovigilance & Materiovigilance
Workshop Details
Date: 26th February 2026
Duration: 1 Day
Nationality: Open to all
Eligibility: Pharmacists & Medical device professionals etc.
Time: 10:30 Hrs to 17:00 Hrs
Mode: Onsite
Venue: Kalam Convention Centre, AMTZ Campus, Visakhapatnam
Course Fee: 2360(Including GST)
đź“ť Last Date for Registration: 20th February 2026
For More Information:
K. Durgankitha
📱 9281078556
📧 durgankitha.k@amtz.in
✨ Don’t just report adverse events- be the professional who safeguards lives..!
For payment scan this QR code WhatsApp the payment screenshot to 9281078556 or 8897330990
| S.No | Start Date | End Date | Total Amount (INDIA) | Total Amount (Foriegn) |
|---|---|---|---|---|
| 1 | 2026-02-10 | 2026-03-31 | 2,360 | 50 |
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