Advance Your Regulatory Skills – Empower Global Compliance!
Become EU MDR–ready and elevate your role as a Global Medical Device Professional!
Training Modules:
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General Overview of EUMDR
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Classification of Medical Devices
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Economic Operators
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Quality Management System (QMS)
Requirements
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Technical Documentation
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Clinical Evaluation & Investigation
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Conformity Assessment
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UDI and EUDAMED
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Labelling and Instructions for Use (IFU)
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Post-Market Surveillance (PMS)
Eligibility: Medical Device Manufacturers, Quality and Regulatory Professionals, Service
Providers in Healthcare sector & Researchers/Academicians and Interested UG/PG students.
Mode: Online (Microsoft Teams)
Duration:
2 Days
Date: 26th & 27th September 2026
Timings:
10:30 AM to 06:00 PM
Course
Fee: INR 15,000 (Including GST) for Indians, 200 USD for others
Discount Applicable to AMTZ Manufacturers; AiMeD Members; UdaiMeD Memebers; CII Members; ASSOCHAM Members; PWMAI Members; IBSC Society Members / Partners.
Last Date for registration 20th September 2026
For quotation / nominations send email to
durgankitha.k@gmtu.in
For more information: Contact Ms Durgankith 9281078556
For payment scan this QR code WhatsApp the payment screenshot to 92810 78556 or 8897330990
| S.No | Start Date | End Date | Total Amount (INDIA) | Total Amount (Foriegn) |
|---|---|---|---|---|
| 1 | 2026-04-20 | 2026-12-31 | 0 | 0 |
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