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How to submit an application, data package and responses for proposed or existing marketing authorisations.
When you must report the amount of electrical and electronic equipment (EEE) you place on the market and how to do it.
Submissions related to human medicines need to be submitted directly to the MHRA.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
A research paper from the CMA
The seeds which must be certified before you can market them, how to get them certified and how to get a licence for your seed business.
How to find export opportunities and overseas customers for your business on great.gov.uk: get help selling online overseas, get help from a trade specialist.
How to charge and account for VAT on the movement of goods between Northern Ireland and EU member states (VAT Notice 725).
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Who in the pharmaceutical industry can be a Marketing Authorisation Holder, named distributor or local representative and how to make changes to these.
This playbook explains how we use social media at GDS. In it, we share our best practice, what we've learned and what we're planning to do.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
Processes for marketing authorisations granted before 31 December 2020, or submitted or ongoing from 1 January 2021.
This section provides guidance for communications network providers on legislation, regulation, working with local authorities and with property developers.
How to renew marketing authorisations for products granted through different routes and at different times.
Access online catalogues and get quotes for the procurement of low value goods and services across the public sector.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
Find details of the conditions for using online services, electronic payments and qualifying for incentives.
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