Medical Device Services

Medical device facility

The GMP Group have expanded our expertise into the Medical Device sector to ensure compliance of the regulations in place for their effective manufacture

Medical Device Engineering

With the current expansion in the medical device R&D and manufacturing sectors, The GMP Group have expanded their own expertise in this area. We are therefore well placed to offer design and project delivery to medical device companies.

Medical Device Facility Design for Compliance

Medical Device manufacturing processes are extremely varied due to the number of different products covered under the FDA and EMA regulations. The GMP Group have designed facilities in accordance with FDA21 CFR Part 820, 210 & 211 as well as Euralex Vol 4 and EU Directories for invitro diagnostic, medical devices and active implantable medical devices.

Medical Device Facilities Design & Engineering Capabilities

Although the medical device sector is so diverse in the products coming through R&D and manufacture, The GMP Group core capabilities in space design (clean and support areas), environment, process engineering and critical utilities  and equipment procurement provides a foundation to successfully deliver projects. Our staff will design and manage projects from concept through to manufacturing start up, including process validation.

Contact Us

To speak with us further, or to arange a meeting, please call us on 08450 344 340 or click below to send us an email

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