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Register to vote Register by 18 June to vote in the General Election on 4 July.
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.
Climate change is happening and is due to human activities; along with warming, many other changes are occurring such as melting polar ice, rising sea levels and more frequent floods, droughts and heatwaves.
Using an ecological momentary assessment to evaluate your digital health product.
Helping public health practitioners conducting evaluations – developing a logic model to represent how your intervention works.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Guidance for manufacturers, importers and distributors.
Documents, certificate, letters, and notes available from the British embassy and consulates in the USA.
Find out what reducing parental conflict is and about the work of the Reducing Parental Conflict Programme.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
How to use a quasi-experimental study to evaluate your digital health product.
Investors and businesses may be legally required to tell the government about certain sensitive acquisitions under the National Security and Investment Act.
A brief explainer of some of the key policy areas of the Prisons Strategy White Paper.
This article focuses on one specific evaluation, of an irrigation project in Malawi
Signs that may suggest rabies in bats, what to do if you spot them and measures to prevent exposing yourself to the disease.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
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