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Helping public health practitioners conducting evaluations – what the evaluation is, when it should be undertaken and the different types of evaluation available.
Information and guidance on a range of medical devices for users and patients.
How to use a case-control study to evaluate your digital health product.
The MHRA is ready to provide any assistance for clinical trials applications submitted for COVID-19
How to write up and share your findings
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
The following guidance has been jointly developed by the Heath Research Authority (HRA) and MHRA, in consultation with the Information Commissioners Office (ICO), on behalf of the UK.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
Information about the awards process for applicants, employers, assessors and award holders.
How to carry out a clinical trial to apply for a marketing authorisation, manage your authorisation and report safety issues.
Using an ecological momentary assessment to evaluate your digital health product.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Good clinical practice (GCP) referrals received by the MHRA for 2011 to 2020.
Information from the National Health Service on conditions, treatments, local services and healthy living
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