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This guide provides advice on what the British Embassy can do to help UK nationals affected by domestic abuse in France, the services available in France, how to report abuse to the police and how to get protection.
You can report serious concerns about your employer to us, if you suspect wrongdoing in an area we regulate.
Provides detailed information on both potential types of information and evidence, and the correct way to process and record such information.
Report internet content promoting terrorism, extremism or violence - your report will be treated anonymously.
How the British embassy or consulate can help, including contacting family, UK prison transfers, money transfers and complaining about mistreatment.
Information on how the CMA investigated the merger, and how you can find out more.
Get advice from Natural England to help you comply with laws that protect wildlife and the natural environment.
FCDO travel advice for Venezuela. Includes safety and security, insurance, entry requirements and legal differences.
How to make applications under the Regulation of Investigatory Powers Act (RIPA) and how the government responds to terrorist incidents.
Details of RAIB investigation reports, safety digests, and urgent safety advice published during 2021.
Find out how to get help if you have concerns that someone is being abused or neglected under a lasting power of attorney, enduring power of attorney or deputy court order.
Crime and fraud issues in international trade: theft of goods, money laundering, cyber crime, employee fraud, infringement of intellectual property.
Guidance for prosecutors and investigators on their asset recovery powers under Section 2A of the Proceeds of Crime Act 2002.
Details of RAIB investigation reports, safety digests, and urgent safety advice published during 2022.
The process for applicants applying for a Paediatric Investigation Plan (PIP) modification or waiver.
There has been a compromise to an Armed Forces payment network. This page provides guidance for those affected.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
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