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How product specific rules are used to identify the country of origin when importing or exporting between the UK and EU.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
A summary of the types of scientific advice available at the MHRA, the process for getting advice and the fees involved.
What Works to Prevent Violence against Women and Girls: funding opportunity. Aims to build knowledge on what works to prevent violence against women and girls (VAWG).
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
This guidance explains what rules of origin (RoOs) are and the changes under the Developing Countries Trading Scheme (DCTS).
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to use a quasi-experimental study to evaluate your digital health product.
Information on how the Department for Education (DfE) and its executive agencies share personal data.
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