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Pharmacovigilance system requirements
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Guidance for completing forms ID1: Certificate of identity for a private individual, and ID2: Certificate of identity for a body corporate.
List of vexatious litigants, banned from starting court cases without permission.
Documents, certificate, letters, and notes available from the British embassy and consulates in the USA.
How to send your information to Companies House using our online services.
Use form US-Individual 2002 to apply for relief at source or to claim repayment of UK Income Tax.
If you hold certain information, you should contact OFSI as soon as practicable.
Rules outlining the form, manner of delivery and method of authentication for documents delivered to Companies House in electronic or paper format.
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)’
Send files, pay fees and track cases in the High Court and the upper tribunals.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Statistics on new individual insolvencies in England and Wales, and related statistics for Scotland and Northern Ireland
Guidance for people with symptoms of a respiratory infection including COVID-19, or a positive test result for COVID-19.
How to file annual accounts with HMRC and Companies House
How to complete form P11D if you’re an employer and need to report end-of-year expenses and benefits for employees and directors.
How to request and manage the authentication code you'll need to file information online at Companies House.
Understand the roles of accountable persons and the principal accountable person for a high-rise residential building, and what they must do.
Find out how to report information to HMRC using the Automatic Exchange of Information (AEOI) if you are a financial institution.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
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