Global Excellence in Medical Device Testing
Medical device testing services examine the effectiveness and safety of equipment with medical application(s). They are 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.
When you work with Medical Engineering Technologies you get:
- A partner that operates globally and has over 20 years of experience in device testing
- A team that understands the urgency of your projects
- The benefit of our experience with and knowledge of a wide variety of devices
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 will understand your product, conduct a risk analysis and execute the study with aplomb.
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 offices in the UK and France. We provide testing to clients across the Globe and they sell their products world-wide. When you work with us it will always feel like we are neighbours.
We work to international standards ensuring your compliance where ever you are. This includes the MDR, EMA Guidelines, FDA Guidance, ICH, ISO standards, pharmacopoeias and any national requirements.