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Explains planning controls relating to the storage of hazardous substances in England and how to handle development proposals around hazardous establishments.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
This advice provides information about how an applicant can request a change to a Nationally Significant Infrastructure Project (NSIP) application after it has been accepted for examination, and before the close of the examination.
How to register your medical devices with the MHRA for the markets in Great Britain and Northern Ireland.
Food and drink labelling and packaging regulations - what you must show, warnings, health and organic labels and packaging standards.
Find out details of the Procedure Codes and Additional Procedure Codes (both Union and National) excluded from use with Simplified Declaration Procedure (SDP) with regular use and Entry in Declarants Records (EIDR).
Find out the rules to establish the country of origin of imported and exported goods and to help identify goods which qualify for lower or no Customs Duty.
Investors and businesses may be legally required to tell the government about certain sensitive acquisitions under the National Security and Investment Act.
Find out how you should prepare for a telephone or video court or tribunal hearing and what to expect on the day.
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