Today the medical sector spans over a wide range of applications with the purpose of saving or making our lives better. Some of the challenges within this field are ensuring product quality, IoT integration/data security and of course the cost of product development – all meeting the EU Medical Device Regulation, MDR 2017/745 and US Medical Devise Regulation, 21 CFR: Parts 800-1050. The ISO 13485 standard provides the tools for our organization to manufacture consistent printed circuit boards at a level of quality that our customers then use in their products to help meet applicable regulatory requirements. Please see below for a selection of applications we serve.