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Register to vote Register by 18 June to vote in the General Election on 4 July.
Use this form to complete a ‘statement of information’ to help the court decide whether the financial and property arrangements you’ve made are fair.
Pharmacovigilance system requirements
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Guidance on certain consultation and publicity requirements of the Nationally Significant Infrastructure Project regime.
Find the notes for all Declaration Category Data Set tables covered by Appendix 21-25 of the CDS Declaration and Customs Clearance Request Instructions.
Find out how to prove the originating status of your goods and check if you can claim preferential tariff treatment.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
Use form C&E48 to apply for authorisation to use simplified procedures for importing and exporting.
Find out about safety and security requirements that apply to goods entering and exiting the UK.
When publishing your developer contributions data, follow this guidance on how to format, label and publish the data.
This is an explanation of how we process personal data.
Claim relief on import duty and VAT when importing miscellaneous documents and related articles into the UK.
Get a goods movement reference to move goods through locations which use the Goods Vehicle Movement Service.
How to make an origin declaration if you're using it as proof of origin for products using the Developing Countries Trading Scheme.
How to submit a proposal to the Defence and Security Accelerator
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Helps you find the information you need in the river basin management plans (RBMPs).
Submissions related to human medicines need to be submitted directly to the MHRA.
Marketing Authorisation Holders should review their manufacturing processes to identify and, if found, to mitigate the risk of nitrosamine impurities being present.
How investigators and sponsors should manage clinical trials during COVID-19
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