Do you represent the small company within Medical Device with the big plans?
Now you can take part in a new concept of services and tools at Aptio Group that streamlines your quality assurance from an early start.
We offer various modules in services and tools that become your framework for living up to current requirements within MDR/IVDR, ISO13485 and 21CFR820 (QSReg).
You are welcome to contact us, and we will tell you more
Scroll the images to view what Aptio 13485 QMS has to offer:
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