Making sure your clinical data meets the latest regulatory requirements.
The new medical devices regulation means getting the necessary clinical data to support the efficacy of your device is more important than ever.
We can help answer your questions about how much evidence you need to get your device through approval.
What’s more, we can also put you in touch with specialists to help you run almost any aspect of your clinical trial including:
- Connecting with clinicians to design the protocol
- Developing the ethics committee submission
- Manufacturing the material for clinical trials in our clean rooms
- Recruiting patients to participate in the trials
- Running the trial
- Collecting the data
- Reporting the results
- Compiling your data in a format suitable for the medical devices regulation
World class experts on hand to support your project
Whatever support your project needs, we’re here to help its development. Let’s move things forward, together.
Our unique approach
Our partnerships with the University Hospitals of Derby and Burton and the Nottingham University Hospitals means we are ideally placed to give you the support you need to collect your clinical trial data.
The NHS Trusts are key partners for the design, development and implementation of clinical trials and accessing clinical input and expertise during the product development cycle.
They have access to patient groups and clinicians and can configure clinical trials in line with your specific product development.
When you work with us we’ll oversee the process of working with the various groups involved in running your clinical trial. So you won’t have to manage relationships with several different groups and can take a more integrated approach.
Don’t take our word for it
View our success stories and ongoing projects to show you how MTIF is on the edge of medtech innovation