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Departments, agencies and public bodies
News stories, speeches, letters and notices
Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
Make sure that domains that do not send email cannot be used for spoofing.
How to object to the registration of a lasting or enduring power of attorney - including forms and fees
Guidance to help organisations choose a monitoring approach for stack emissions to air that meets Environment Agency and MCERTS requirements (formerly part of M2).
Apply for a Secondment Worker visa to work for a UK organisation as part of a high-value contract - eligibility, fees, documents, extend, switch or update, bring your partner and children.
When tests to detect COVID-19 are commonly used (use cases) and what to consider when deciding which type of test to employ.
Look up a trade mark to see if something identical or similar to your brand is already registered.
You must tell DVLA if you have a brain abscess, cyst or encephalitis - download the correct form to let them know
How to use A/B testing to evaluate your digital health product.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Information for clinicians and patients.
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
Guidance on how to prove someone’s identity or give them access to your service or organisation.
Advice for medical professionals to follow when assessing drivers with neurological disorders.
The review of the safety of isotretinoin has concluded.
How to carry out a clinical trial to apply for a marketing authorisation, manage your authorisation and report safety issues.
You must include the appropriate legal basis for your application when you apply to MHRA for a marketing authorisation.
How to contact MHRA for specific services or enquiries.
Use the rolling review route when you want to submit your eCTD dossier in separate parts for pre-assessment instead of making a full consolidated document submission.
How to apply for repayment of import duty and VAT on protective equipment or medical supplies brought into the UK from non-EU countries from 30 January 2020 up to 31 December 2020.
You can make observations on the patentability of a published patent application.
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