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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 Foreign, Commonwealth & Development Office (FCDO) provides lists of English-speaking lawyers abroad to help British nationals find the legal support they need.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Guidance on Animal Test Certificates (ATCs) required to carry out the field trial of a veterinary medicine in animals (clinical trial) in the UK.
Apply for a Temporary Work – Government Authorised Exchange (GAE) visa for work experience, training, research or fellowship - eligibility, extend or switch, family members
How to conform with the legal requirements for placing medical devices on the market.
Check if you need a tuberculosis (TB) test to support your visa application and find an approved clinic in your country
Guidance and application forms for Marketing Authorisations, Animal Test Certificates, Veterinary Homeopathic Remedy, Export and Import certificates, Batch release and Batch control.
Submissions related to human medicines need to be submitted directly to the MHRA.
Advice on writing clear notices and maximising replies to your FSNs.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
Details of General Licences issued by OFSI
The actions to take for sourcing medicines in different circumstances.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Don’t include personal or financial information like your National Insurance number or credit card details.
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