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A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
Find out how to declare that your goods have been put to their authorised use, destroyed or re-exported.
Get certified or uncertified copies of your patent, trade mark or design registration documents to prove that you have intellectual property rights.
You can get copies of documents if you need to prove who owns or has…
Use patents form 23 to apply for either a certified or uncertified copy of…
Use form TM31R to get a certified copy of a trade mark. Certified copies…
Use form DF23 to request a certified copy of a design registration or…
Certify a document as a true copy of the original by getting it signed and dated by a professional person, like a solicitor
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
Details of the exceptions to copyright that allow limited use of copyright works without the permission of the copyright owner.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
If the UKCA marking applies to products you manufacture or supply, you will have specific obligations and responsibilities for compliance, depending on your role.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
Buy or get someone's permission to use a patent, trade mark, design or work under copyright
Find out more about getting authorised consignor or consignee status to start or end transit movements at your own premises.
Paper prepared by Imperial College London.
Check if you can apply for Authorised Use relief to reduce your payments when you import goods for a specific use. This can include repairs, maintenance or processing.
The approach the MHRA intends to take for products approved or pending in decentralised procedure (DCP) or mutual recognition procedures (MRP).
Apply for your site to be approved to host heavy goods vehicle (HGV) or Driver Certificate of Professional Competence (CPC) part 4 tests.
How to get a parallel import licence for your medicine in the UK, including pharmacovigilance requirements and submitting your application.
The way you apply to licence biological products has changed
The MHRA has authorised cabotegravir as 30 mg tablets and as a 600 mg long-acting injection administered every two months
You can claim a relief to pay less Customs Duty and VAT if you re-import goods to the UK.
Don’t include personal or financial information like your National Insurance number or credit card details.
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