Medical Device Development
During medical device development, medical devices move from the design stage to ensure the medical devices are fit for purpose.
Meridian's medical device development ensures all medical devices meet the exact needs of our clients and we work through any validation, verification and standardisation requirements for the medical devices.
During medical device development, we work to 93/42/EEC - the CE mark for medical device manufacturing and the standard to ensure all medical devices are safe. The medical devices also adhere to ISO 13485 as part of medical device manufacture certification.
Medical devices progress from design through CAD to development and then onto the manufacture of the medical devices themselves. This stringent process ensures all medical devices provide customer satisfaction from the highest quality workmanship available.
The medical device development stage forms part of the overall medical equipment validation process which provides reassurance that every standard has been met.