Working with our partners to design and manufacturer custom-built medical devices, medical grade parts, and components for use in medical and point-of care diagnostic healthcare environments.
We have implemented strict regulatory requirements to ensure consistent design and manufacturing procedures are followed throughout our manufacturing sites.
The design, manufacture and build of medical technologies is tightly regulated in the European Union. Before a medical technology can be legally placed on the EU market, a manufacturer must comply with the requirements of all applicable EU legislation and affix a CE mark to their device.
PCML Group Cambridge are ISO 13485 certified to manufacture and assemble a range of medical grade devices and components.
Working with one supplier simplifies the supply chain. PCML can manage all your engineering and product assembly requirements.
Contact us on 01223 293904 for more information
PCML manufacture and build a range of medical devices - working closely with our customers to ensure your products are ready for market in the shortest possible lead times.
