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Register to vote Register by 18 June to vote in the General Election on 4 July.
Claim relief on import duty and VAT when importing miscellaneous documents and related articles into the UK.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
All specifications for the packaging of all Higher Activity Waste (HAW)
Find out what goods you do not value when when working out the VAT due on import to the UK.
Guidance for manufacturers, importers and distributors.
Find out what information you must send with a transfer of funds if you’re a payment service provider.
This page contains Nuclear Waste Services (NWS) Waste Package Specifications and Guidance for waste packages destined for geological disposal.
We work with organisations across the UK that produce radioactive waste.
How to send your information to Companies House using our online services.
You should follow the standard file process outlined below when submitting work for online and paper billing.
Under the Public Records Act, the Foreign, Commonwealth & Development Office must transfer files selected for permanent preservation to The National Archives.
The MHRA is continuing to accept Active Substance Master Files (ASMFs) and Certificates of Suitability (CEPs)
How to submit an application, data package and responses for proposed or existing marketing authorisations.
How to package medicines for sale and what information you must provide to consumers and healthcare professionals.
Example files for sponsors using bulk data transfer to send information from their IT systems to the sponsorship management system.
MCA interpretation of the certification and vehicle/container packing certificate requirements of the International Maritime Dangerous Goods (IMDG) Code.
How UK organisations that supply or import packaging should comply with extended producer responsibility (EPR) for packaging.
How to structure your packaging data submission. It includes information about the different types of data you need to submit and the codes you need to use.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
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