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Find information on completing the UK property and other property sections of your Self Assessment tax return.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
A summary of the types of scientific advice available at the MHRA, the process for getting advice and the fees involved.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
The Scientific Advisory Committee on the medical implications of less-lethal weapons (SACMILL) provides independent advice to UK government departments and organisations on the biophysical, biomechanical, pathological and clinical aspects of less-lethal weapon systems. SACMILL is an advisory non-departmental public body,...
Data First is a pioneering data-linking, research and academic engagement programme led by the Ministry of Justice and funded by ADR UK.
Submit your research to Athena; Dstl's central repository of MOD-sponsored scientific and technical research reports.
Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
Guidance for people with symptoms of a respiratory infection including COVID-19, or a positive test result for COVID-19.
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