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Advice and guidance on the health needs of migrant patients for healthcare practitioners.
Marketing standards for poultry meat producers, manufacturers, retailers and distributors.
Find out about applying for the Spirit Drinks Verification Scheme, how to submit brand information, fees and making sure your production process is compliant.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Licences and authorisations to import genetic material, research and diagnostic samples, trade samples and display items, and some live animals and animal products.
Information for healthcare professionals on how pulse oximeters are regulated, home use and issues to look out for when using the devices
The New Active Substance Work Sharing Initiative (NASWSI) has successfully approved several medicines through this international collaboration and continues to foster cooperation and strong relationships between its Access partners. The Biosimilar Work Sharing Initiative (BSWSI) builds on this success.
A list of upcoming webinars on the UK’s approach to product marking and placing products on the market in Great Britain and Northern Ireland.
This guide is to help you and your business understand issues around data protection and privacy. It is intended for organisations that provide online services likely to be accessed by children.
A patient alert card is being introduced for men taking finasteride to help raise awareness of the risk of psychiatric side effects and sexual dysfunction, including the potential for sexual dysfunction to persist after treatment has stopped. Healthcare professionals are...
What you need to know about and do to comply with the law and keep consumers safe.
Joint Statement delivered by Zambia on behalf of 81 Member States including the United Kingdom at the UN General Assembly.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
The Medicines and Healthcare products Regulatory Agency regulates medicines, medical devices and blood components for transfusion in the UK. MHRA is an executive agency, sponsored by the Department of Health and Social Care .
Agreed responsibilities and expectations with regard to the supply of age restricted products and services.
Information relating to the Tobacco and Vapes Bill which was introduced in the House of Commons on 20 March 2024.
We’re working to help people securely prove who they are without having to rely on physical documents.
Use these general provisions to help you determine the origin of your products.
Using an ecological momentary assessment to evaluate your digital health product.
Don’t include personal or financial information like your National Insurance number or credit card details.
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