Global Excellence in Medical Device Testing

Medical device testing services examine the effectiveness and safety of equipment with medical application(s). It is used to generate data to support product claims and regulatory submissions. This validation is applied to all classes of active devices, non-active devices, and drug delivery combination products. Careful protocol development and implementation can ensure effective and efficient execution of the test programme. An ISO/IEC 17025 accredited Quality Management System, combined with good training and logic provides accurate results and reporting. In addition to this, the reason to choose MET as your partner laboratory is our detailed knowledge of a wide variety of devices. We will understand your product, conduct a risk analysis and execute the study with aplomb.

Whether you have a new product development, want to work with the recent changes to ISO 10993, or need to comply with regulations, FDA or the new MDR, we can provide your safety and performance evidence.

Medical Engineering Technologies provides complete confidence from a single source with experience of medical device testing since 1997.

Testing includes: initial consultancy, EMC testing, packaging validation, physical testing, toxicity studies, and toxicity risk analysis.



"We have been using MET’s pilot production facility for 6 months. All the staff at MET have been exceptionally flexible and helpful. We went from initial enquiry to full production in two weeks, then ramped processing up and down at short notice with full co-operation. MET also helped improve processes and quality, and even suggested cost savings. It would be difficult to improve on this service, but MET managed it by providing, an equally responsive and complete analytical chemistry facility in the same building. This enabled us to verify what we were making, develop process improvements, check for contaminants and residuals, and carry out stability studies with ease and grace. Exemplary service, thank you MET you met all our deadlines and demands!"


"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"


"Medical Engineering Technologies Ltd. focuses on providing engineering and scientific solutions to the medical device, biotech and pharmaceutical industries. Besides a medical device testing laboratory, they also offer outstanding support throughout R&D, production and quality assurance"


"I feel totally happy with the relationship between our company and MET, I would highly recommend their service. The staff are always happy to accommodate, friendly and do the utmost to assist us in whatever task we throw their way"


Feb 28, 2019 |
MET News,  |

Published in January, ISO 11040-6:2019 Prefilled syringes -- Part 6: Plastic barrels for injectables and sterilized sub assembled syringes ready for filling, has several changes from previous versions.

Feb 26, 2019 |
MET News,  |

MET’s new laboratories will be opened at 11am on the 5th of April 2019 by Lord Pickles. Former member of the UK Parliament, the Right Honourable Eric Pickles has been   Secretary for Communities and Local Government. He is now also the Chairman of the Parliamentary Review (a series of publications which are intended to promote best practice in business). 

Feb 13, 2019 |
MET News,  |

As part of MET’s laboratory expansion programme we are adding a dedicated physical performance testing area to implement dose accuracy studies and design validation of drug delivery devices. The new area will have 21 CFR part 11 compliant tensile equipment and balances for GMP studies. There will also be an isolation area for testing of syringes and cartridges containing cytotoxic drugs.