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 25 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 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, biological evaluation plans, human factors studies, packaging validation, physical testing, chemical characterisation and biocompatibility studies, and toxicity risk analysis.
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.
When you work with MET you get reliable, trusted and accurate testing, supporting the creation of Medical devices for safe patient use.
We provide testing to clients across the Globe and they sell their products world-wide and yet it will always feel like we are your neighbours.
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.
MET's laboratory services are available in the UK and France
There is no need to worry about Brexit. We work to international standards. Our systems are and will be equally recognised by Notified Bodies and other regulatory authorities because none of the rules for medical device validation change, as they are not UK dependent. The MDR will still apply to all medical devices made in the UK and our services will still test to the EMA Guidelines, FDA Guidance, ICH, ISO standards, pharmacopoeias, and any national requirements. We provide testing to clients across the globe, who sell their products world-wide. You can still benefit from our super-efficient service and fantastic turnaround times (we receive samples from around the world without customs delays). If you do have any worries, please feel free to contact our team.