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.