Advance Your Regulatory Skills – Empower Global Compliance!
Become EU MDR–ready and elevate your role as a Global Medical Device Professional!
Training Modules:
Ø
General Overview of EUMDR
Ø
Classification of Medical Devices
Ø
Economic Operators
Ø
Quality Management System (QMS)
Requirements
Ø
Technical Documentation
Ø
Clinical Evaluation & Investigation
Ø
Conformity Assessment
Ø
UDI and EUDAMED
Ø
Labelling and Instructions for Use (IFU)
Ø
Post-Market Surveillance (PMS)
EEEligibility:Medical Device Manufacturers, Quality and Regulatory Professionals, Service
Providers in Healthcare sector & Researchers/Academicians.
Mode: Online
Duration:
2 Days
Date:
30th & 31st of October 2025
Timings:
10:30am to 06:00pm
Course
Fee: INR 15000 for Indians, 200USD for others
Last Date for registration 25th October
2025
For quotation / nominations send email to
durgankitha.k@amtz.in
For
more information:
K.Durgankitha
Scientist-A,
IBSC
Mobile:
7013028578
For payment scan this QR code WhatsApp the payment screenshot to 7013028578 or 8897330990
| S.No | Start Date | End Date | Total Amount (INDIA) | Total Amount (Foriegn) |
|---|---|---|---|---|
| 1 | 2025-10-16 | 2025-12-31 | 15,000 | 18,000 |
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