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How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
RAIB investigation reports, safety digests, and urgent safety advice by year of publication.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to approach sampling ambient air and the sampling and analytical techniques to use.
Submit your research to Athena; Dstl's central repository of MOD-sponsored scientific and technical research reports.
How to use a quasi-experimental study to evaluate your digital health product.
Resources to help local commissioners achieve value for money by estimating the return on investment (ROI) and cost-effectiveness of public health programmes.
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