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Documents, certificate, letters, and notes available from the British embassy and consulates in the USA.
How someone in Poland can get documents prepared, witnessed or certified, take an oath of British citizenship and obtain informative notes.
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Check the regulations on aircraft parts imported with a certificate of airworthiness.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
How to conform with the legal requirements for placing medical devices on the market.
How to apply for marketing authorisation via this new procedure.
Check if you need a tuberculosis (TB) test to support your visa application and find an approved clinic in your country
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Details of General Licences issued by OFSI
Submissions related to human medicines need to be submitted directly to the MHRA.
A summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices.
Find registered patents, patent applications and pending patents
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Use these forms if you import, export, or move goods through the UK.
Pharmacovigilance system requirements
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
You may need a visa to come to the UK to visit, study or work.
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