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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.
How to conform with the legal requirements for placing medical devices on the market.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
Advice on writing clear notices and maximising replies to your FSNs.
A checklist from the Foreign, Commonwealth & Development Office to help British people prepare for travelling and staying safe abroad.
How someone in Poland can get documents prepared, witnessed or certified, take an oath of British citizenship and obtain informative notes.
Details of General Licences issued by OFSI
UK Health Security Agency (UKHSA) culture collections offer a range of products and services for medical science and laboratory healthcare use.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Submissions related to human medicines need to be submitted directly to the MHRA.
Apply for a higher education course, track your application and accept or reject your offers.
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