The GMP Group have expanded our expertise into the Medical Device sector to ensure compliance of the regulations in place for their effective manufacture
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 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.
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.
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
Speak to one of our Medical Device Facility Experts
Call 08450 344 340
Medical device services include
