ISO 13485 and It's Significance in the Medical Devices Domain
ISO 13485 is a quality management system (QMS) standard specifically designed for medical device manufacturers. It outlines the requirements for the design, development, production, and delivery of medical devices, as well as the monitoring and control of associated processes.
ISO 13485 is critical in the medical device domain. It provides a framework for manufacturers to ensure that their products consistently meet regulatory requirements and customer demands.
Compliance with ISO 13485 can help companies gain regulatory approval for their products in multiple markets. It ultimately helps to increase their competitiveness and market access.
What we covered in this webinar:
• Overview of Quality Management System
• Introduction & significance of ISO 13485
• Why you should be compliant with ISO 13485
• Demonstration on how ISO helps Medical Devices to improve their quality.
Some key benefits of ISO 13485 include:
ISO 13485 is therefore crucial for medical device manufacturers to ensure the quality and safety of their products and get global market access.
Please watch the full webinar to learn more about applying ISO 13485 to medical devices.
This webinar was presented by Decos, a cutting-edge technology services partner ready to meet your diversified needs in the healthcare domain.
If you have any questions about this webinar or wish to seek advice on ISO13485 for your healthcare project, please contact Devesh at devesh.agarwal@decos.com
We would love to discuss it with you!