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Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
Advice for employers carrying out right to work checks during the coronavirus pandemic.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
You have the right to get a copy of the information that is held about you. This is called the 'right of access'.
What detailed information you need to send to HMRC to support your Research and Development (R&D) tax relief claim, and when and how to submit it.
What packaged goods are, how they are labelled, units of measurements used and compliance with weights and measures regulation.
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.
Employment rates for different ethnic groups in England, Wales and Scotland.
Submissions related to human medicines need to be submitted directly to the MHRA.
Information for employers on checking EU, EEA and Swiss citizens’ right to work.
What the public register is, what details you need to give us, and how the public can access this information.
If you're advertising or marketing, including direct marketing, you must be accurate and honest and follow the advertising codes of practice
Foreign, Commonwealth & Development Office (FCDO) advice for lesbian, gay, bisexual and transgender (LGBT+) people travelling abroad.
Comply with good pharmacovigilance practice and prepare for an inspection.
A collection of guidance to help landlords, homeowners and letting agents carry out correct right to rent checks and avoid civil penalties.
This guide sets out who has to apply for a permit, how to apply and explains the other rules covering travel to Antarctica.
Information about the UK’s points-based immigration system for EU, EEA and Swiss citizens.
This collection gathers together datasets that were provided in response to FOI (Freedom of Information) requests.
Keep up to date with the latest information from the UK GLP monitoring authority.
Guidance on handling sensitive information in IT.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
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