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The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
How to conform with the legal requirements for placing medical devices on the market.
How to use a combination of quantitative and qualitative data to evaluate your digital health product.
Advice on writing clear notices and maximising replies to your FSNs.
The Foreign, Commonwealth & Development Office (FCDO) provides lists of English-speaking lawyers abroad to help British nationals find the legal support they need.
Apply for a Temporary Work – Government Authorised Exchange (GAE) visa for work experience, training, research or fellowship - eligibility, extend or switch, family members
Apply for a Temporary Work – International Agreement visa if you're working under international law (including diplomatic households) - extend or switch, family members
The epidemiology, symptoms, diagnosis and management of human T-cell lymphotropic virus types 1 and 2 (HTLV-1 and HTLV-2).
Submissions related to human medicines need to be submitted directly to the MHRA.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Apply for a higher education course, track your application and accept or reject your offers.
Guidance for people with symptoms of a respiratory infection including COVID-19, or a positive test result for COVID-19.
Details of General Licences issued by OFSI
A summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Find registered patents, patent applications and pending patents
Information for entertainers and musicians, from non-visa national countries, such as EU Member States and the US, visiting the UK for performance and work.
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