Medical Engineering Technologies Ltd
Excellence in laboratory analysis - efficiently delivered
Device Testing
MET prides itself on delivering excellence in medical device testing. We offer facilities and control processes that rigorously challenge devices against regulatory requirements, industry quality standards and clients' product claims. We analyse regulatory obligations then devise and implement test programmes in the shortest possible time frame. With biocompatibility testing (ISO 10993), functional testing and post-marketing surveillance, we have helped young development companies and established multinational manufacturers alike for many years. Involved early in your project, we can ensure efficient progression, by highlighting aspects that require protracted testing or areas likely to require material changes or redesign work. Read more...
Packaging Testing
Experienced in validating medical device packaging since 1997, MET has helped many manufacturers fulfil regulatory requirements to demonstrate product shelf-life and the effectiveness of packaging as a sterile barrier for their devices. Our ISO 9001-2008 accredited laboratory facilities include accelerated ageing ovens, seal strength and integrity testing equipment (peel testers, burst and leak testers, dye penetration) and transport simulation studies. We undertake assessments on pouches, blisters, Tyvek®, foil or paper for all classes of devices. Read more...
Equipment
Cost effectiveness, robustness and reliability are at the heart of all the packaging and quality assurance equipment we sell. Machines are designed for clean-room production and will dependably deliver fully validated packs over many years. Our range includes 4-sided-seal pouch making and sealing machines running from 25 to 125 cycles per minute, blister tray formers and sealers, tensile testers as well as burst and leak testers. Validation and maintenance services complement the range. Read more...
Consulting
Project management, product design and testing, regulatory support: just some of the consultancy services from MET. Our team have worked with a wide range of medical devices and we include project managers, device designers and scientists. Our regulatory consultants support your team in compiling technical files and product registration. In addition our experts can work up your ISO 13845 systems and paperwork, provide training in its implementation and conduct pre-assessment audits. Read more...
Here is some more feedback from our clients:
Everyone at MET felt like part of our own team. They spent the time required to understand our needs and made sensible project proposals within our budget and time requirements, which completely fulfilled our regulatory needs. We are still working and I will continue to work with MET. I would highly recommend their services.
Proprietor, an innovative medical device development company
MET are a fantastic company and a great supplier. We have a fantastic relationship with them and long may it continue.
Laboratory Manager a well known medical device company
The service that MET provides at the moment is excellent and I would just like to thank Angela Bell and Mark Turner again.
Design Director, Bone substitute manufacturing company
