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Check what you need to do to sell cosmetic products in Great Britain.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Apply for a Temporary Work – Government Authorised Exchange (GAE) visa for work experience, training, research or fellowship - eligibility, extend or switch, family members
Information to support your recovery after COVID-19.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
How to use a randomised controlled trial to evaluate your digital health product.
Consultation launched on proposals to expand scheme to 1.6 million more people to help tackle tooth decay.
Get help to classify cigarettes, cigars, raw tobacco, smoking tobacco, tobacco for heating and nicotine substitutes for import and export.
Information for clinicians and patients.
Information for under 18s and their parents or guardians on the Botulinum Toxin and Cosmetic Fillers (Children) Act 2021.
Information on how to report a serious undesirable effect (SUE) or safeguarding issue for cosmetic products.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Check the tariff classification for bones with some meat, fat and tendons (so called soup bones).
Product Safety Report for Teeth Whitening Kit presenting a serious chemical risk.
How practitioners and businesses can comply with the Botulinum Toxin and Cosmetic Fillers (Children) Act 2021.
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