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Register to vote Register by 18 June to vote in the General Election on 4 July.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Documents, certificates, services available at British Embassy in Manila.
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.
Guidance on certain consultation and publicity requirements of the Nationally Significant Infrastructure Project regime.
How to apply for marketing authorisation via this new procedure.
How to apply to become an authorised consignor or consignee, and get authorised for other transit simplifications.
Documents, certificates, letters and notes available at the British Embassy Albania.
Guidance on the decentralised and mutual recognition reliance procedure (MRDCRP) for marketing authorisation applications including information on how to apply.
Ofqual's formal legal list of Regulatory Documents (documents containing additional rules and guidance for regulated qualifications).
Answers to frequently asked questions on Approved Document F, which sets standards for ventilation in new dwellings.
Check the regulations on aircraft parts imported with a certificate of airworthiness.
How to import animals and animal products to Great Britain (England, Scotland and Wales), the Channel Islands and the Isle of Man from non-EU countries.
Information on the accessibility of the Primary Authority Register for users.
An update on building regulations and fire safety guidance as part of wider reforms to building safety.
How someone in Germany can get documents legalised, witnessed or certified, take an oath, affirmation or affidavit and obtain informative notes on UK naming law
Answers to frequently asked questions on Approved Document S, which sets standards for installation of electric vehicle charge points or cable routes.
How the DSA conducts its activity and what can be expected from its outputs.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Guidance for holders of Marketing Authorisations approved in Northern Ireland or the EU/EEA member states who want to bring a product to market in Great Britain.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
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