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During her PhD, Molly Bartlett took on a 3-month UKRI internship with the Government Office for Science (GO-Science), leading a high-profile project evaluating the impact of the UK’s Chief Scientific Advisers (CSAs).
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
A summary of the types of scientific advice available at the MHRA, the process for getting advice and the fees involved.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How product specific rules are used to identify the country of origin when importing or exporting between the UK and EU.
DCMS invites users' views on proposals for the future of the Taking Part survey.
A guide to collecting data about your packaging. This is for UK organisations affected by extended producer responsibility (EPR) for packaging.
A collection of RPC opinions relating to impact assessments which government departments have now published - published May 2014
Seeking views on current restriction to open access land at Hulne Park in Northumberland and how to submit your comments.
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