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The Foreign, Commonwealth & Development Office (FCDO) provides lists of English-speaking lawyers abroad to help British nationals find the legal support they need.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
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 apply for marketing authorisation via this new procedure.
How to conform with the legal requirements for placing medical devices on the market.
The Export Control Joint Unit (ECJU) administers the UK’s system of export controls and licensing for military and dual-use items. ECJU is part of the Department for Business and Trade .
Advice on writing clear notices and maximising replies to your FSNs.
Apply for a Temporary Work – Government Authorised Exchange (GAE) visa for work experience, training, research or fellowship - eligibility, extend or switch, family members
Submissions related to human medicines need to be submitted directly to the MHRA.
Details of General Licences issued by OFSI
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.
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