A. P. Lyon

The ever-changing medical device regulatory environment places design and manufacturing companies in the unenviable position of allocating valuable resources from active projects to focus on the strategic alignment of their organization and products with.

A.P.LYON offers a solution for medical device companies engaged in the manufacture and global distribution of medical devices to ensure compliance with FDA, MDR EU 2017/745 and ISO 13485 requirements governing the process of complaint handling, reporting.

A.P.LYON offers a solution for medical device companies engaged in the design, development and manufacture of medical devices to help them comply with FDA and ISO 13485 requirements.

A.P.LYON offers a solution for medical device companies engaged in the design and development of medical devices to help them comply with FDA and ISO 13485 requirements.

The new European Medical Device Regulation (MDR) EU 2017/745 lays down rules concerning the placing on the market of medical devices for human use.