HRC in Diagnostic and Technology Evaluation: Regulatory Advice Questionnaire
Opportunity to help shape the regulatory support we provide to the health technology industry
Understanding medical devices and in-vitro diagnostics regulation can be difficult for health technology developers. There can be uncertainty around what laws apply, and how you can ensure you comply with them without delaying getting your device to the market.
We help developers by providing regulatory support and advice to identify what is needed, and how you can best move your device towards the market and NHS adoption.
To do this though, we need to understand what we do well, and where there are gaps in the support we offer.
We have developed a questionnaire so we can better understand the needs of health technology developers in this area.
By completing this short survey, you will help us tailor our support to what you really need and allow us to provide a more effective regulatory support and guidance service.
The questionnaire should take no more than 10 minutes to complete and will remain open until Thursday 18 September.
Here is a link to the questionnaire: https://forms.office.com/e/NYpfz3q0cq
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