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Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
Guidance on the pre-application stage for Nationally Significant Infrastructure Projects.
Submission dates and how the submissions using the EC decision reliance procedure work.
Accounting Officer Assessment summaries for VOA's major programmes and projects.
Blogs where government organisations talk about their work and share information and ideas.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
How to conform with the legal requirements for placing medical devices on the market.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Information for entertainers and musicians, from non-visa national countries, such as EU Member States and the US, visiting the UK for performance and work.
Apply for a higher education course, track your application and accept or reject your offers.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Check the regulations on aircraft parts imported with a certificate of airworthiness.
Pharmacovigilance system requirements
Make sure that domains that do not send email cannot be used for spoofing.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
What you need to do to work and operate in the aviation industry.
Use this form to transform your Madrid Protocol Designation to a UK Trade Mark application.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Guidance for organisations involved in any aspect of the pharmaceutical lifecycle or GLP studies regulated by MHRA, covering the approval of paper documents when working from home
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
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