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Reports, analysis and official statistics
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Data, Freedom of Information releases and corporate reports
A summary of the types of scientific advice available at the MHRA, the process for getting advice and the fees involved.
Information about when you need to submit substantial amendments to a clinical trial including changes to the trial sponsor or legal representative, Investigational medicinal product certification and importation.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
You must get permission to export certain drugs and medicines.
How to approach sampling ambient air and the sampling and analytical techniques to use.
How to apply for a certificate of free sale to export medical devices outside the UK.
Find the residency status of your members to give them the right tax relief using relief at source.
Find out where SPZs are, what defines the different zones and why the Environment Agency must protect groundwater from pollution.
How marketing authorisation holders should inform MHRA of a signal or an ADR to a medicine.
Find out which radioactive sources you need a licence to export and how to apply for one.
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