ISO 13485: Quality Management System for Medical Device

ISO 13485: Medical Device Quality Management System for Medical Devices
The ISO 13485 standard requirements are the foundation upon which a robust quality management system is build for Medical device industry.
This approach is entirely consistent with the requirements for all recognized QMS accreditations. Working with senior management, we ensure the QMS delivers real, tangible benefits to your organization.
Through implementation of an ISO 13485:2016 compliant Quality Management System will enable your organization to identify risk relating to possible non-conformances and reduce or prevent costly incidents.
Product non-conformances with medical devices could literally become a matter of life and death.
Establishing a robust ISO 13485:2016 compliant Quality Management System is a powerful way to demonstrate your organization’s commitment to product quality.
This may also enhance your public image, increase your brand equity and improve your market share. Implementing any new process or system requires commitment. Commitment of resources, time and at times capital investments.
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[@jorgenspetnatz9838]

What do MRM and CAPA mean?
Thanks in advance

[@MavenProfconServicesLLP]

Hello,
MRM = Management Review Meeting
CAPA = Corrective Action & Preventive Action.

[@jorgenspetnatz9838]

@@MavenProfconServicesLLP Thanks so much