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Data, Freedom of Information releases and corporate reports
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 carry out a clinical trial to apply for a marketing authorisation, manage your authorisation and report safety issues.
Apply for a higher education course, track your application and accept or reject your offers.
Submissions related to human medicines need to be submitted directly to the MHRA.
Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
The characteristics, diagnosis and management of Candida auris (C. auris).
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Details of General Licences issued by OFSI
Definitive fees charged for applications under Schedule 7 of the Veterinary Medicines Regulations 2013.
How to apply for, update and cancel licences for the manufacture, import and wholesale of human and veterinary medicines.
The actions to take for sourcing medicines in different circumstances.
Find registered patents, patent applications and pending patents
A summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices.
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