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Submission dates and how the submissions using the EC decision reliance procedure work.
Applications received to amend the specification of a patent under sections 27 and 75 before the court and the Office.
Work out the VAT liability of goods and services supplied by health and care institutions and providers of non residential care to children.
Use a global project licence to simplify the export of military goods and technology classed as collaborative defence projects.
Guidance on the decentralised and mutual recognition reliance procedure (MRDCRP) for marketing authorisation applications including information on how to apply.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
The Intellectual Property Office offers different methods of accelerating the processing of your patent application.
Blogs where government organisations talk about their work and share information and ideas.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How to apply for marketing authorisation via this new procedure.
Pharmacovigilance system requirements
How to conform with the legal requirements for placing medical devices on the market.
To protect your patent outside of the UK, you usually need to apply in each country you want protection in.
Check if you need a tuberculosis (TB) test to support your visa application and find an approved clinic in your country
Definitive fees charged for applications under Schedule 7 of the Veterinary Medicines Regulations 2013.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Submissions related to human medicines need to be submitted directly to the MHRA.
Apply for a higher education course, track your application and accept or reject your offers.
Details of General Licences issued by OFSI
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