Verification of design outputs is a very important part of a medical device's technical file. MET has the device testing facilities and control processes to rigorously challenge your product. We will analyse the regulatory requirements and implement a test programme in the shortest possible time frame.
MET can handle all aspects of your project from concept to production.
Medical Device Development Services
We have very experienced project engineers on hand to fast-track your projects. Comprehensive support is provided by designers, clinicians and academic experts to deliver a superb, validated design package.
| Concept Generation | |
| Prototyping and proving | |
| CE Marking and FDA submission | |
| Production Implementation |
Bench Testing Services
We offer in-house testing programs that can be designed to assess products against either the relevant regulatory standards or your own custom-made testing regime.
| Product Functionality | |
| Verification of Key Product Claims | |
| Independent Investigation of Customer Feedback | |
| Comparative Studies |
One laboratory service that is particularly useful is our product returns assessment – First Line QA. Our laboratory rapidly decontaminates and analyses returns complaints, helping you turn a complaint into a sales opportunity.
Pack Validation & Ageing Trials
Providing proof that your pack maintains product sterility for the duration of its shelf life can be a problem.
MET provides a validation solutions for both shelf life claims and the rigours of shipping
Our accelerated ageing and testing regimes provide comprehensive support documentation for pack integrity and seal strength. Transit trials provide full independent reports following analysis the performance of your packaging.
MET provides a validation solutions for both shelf life claims and the rigours of shipping
Our accelerated ageing and testing regimes provide comprehensive support documentation for pack integrity and seal strength. Transit trials provide full independent reports following analysis the performance of your packaging.
| Simulated Transit Trials | |
| Accelerated Ageing | |
| Leak Testing | |
| Burst Testing |
Regulatory Advisory Service
In today’s regulatory requirement maze, we will smooth the path and help you improve efficiency, meet your regulatory obligations and speed your time to market.
| ISO 9000 Consultancy | |
| ISO 13845 Consultancy | |
| FDA 510K and PMA Submissions | |
| CE Marking and Technical Files | |
| FDA QSR Consultancy |
Contact Us for a discussion about our capabilities or for a quotation.




