Enhance Medical Device Usability and User Experience, analyze and design Inputs and Outputs in accordance with Regulatory Compliance
ELIGIBILITY: Medical Device Manufacturers and Startups, Quality and Regulatory Professionals & Research and Development Professionals, Research scholars & Interested students.
DURATION: 1 DAY (12TH SEPTEMBER 2024)
Key Learning Objectives:
Gain a comprehensive understanding and overview of the medical device design and development process
Learn how a new device is designed and developed from beginning to end with the regulatory requirements and standards
Understand how risk should be managed during the design and development
Discover how development influences clinical evaluations, manufacturing, human factors and usability
Design and Development documentation of the device as per Cl. 7.3 of ISO 13485: 2016
For More details,
Please contact:
Mr. N. Nitturi Naresh Kumar
Head- Trainings Division
+91 8897330990
| S.No | Start Date | End Date | Total Amount (INDIA) | Total Amount (Foriegn) |
|---|---|---|---|---|
| 1 | 2024-11-01 | 2024-12-31 | 5,000 | 12,500 |
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