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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.
How to make an origin declaration if you're using it as proof of origin for products using the Developing Countries Trading Scheme.
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.
When publishing your developer contributions data, follow this guidance on how to format, label and publish the data.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Helps you find the information you need in the river basin management plans (RBMPs).
Get a goods movement reference to move goods through locations which use the Goods Vehicle Movement Service.
How to submit a proposal to the Defence and Security Accelerator
Claim relief on import duty and VAT when importing miscellaneous documents and related articles into the UK.
Submissions related to human medicines need to be submitted directly to the MHRA.
The review of the safety of isotretinoin has concluded.
Use form C&E48 to apply for authorisation to use simplified procedures for importing and exporting.
Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
Find out if you need to use the UKCA (UK Conformity Assessed) marking on products you manufacture or handle.
How investigators and sponsors should manage clinical trials during COVID-19
How to apply for marketing authorisation via this new procedure.
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