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Data, Freedom of Information releases and corporate reports
Documents, certificate, letters, and notes available from the British embassy and consulates in the USA.
Submission dates and how the submissions using the EC decision reliance procedure work.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
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 someone in Poland can get documents prepared, witnessed or certified, take an oath of British citizenship and obtain informative notes.
Advice on writing clear notices and maximising replies to your FSNs.
Apply for a higher education course, track your application and accept or reject your offers.
Guidance for local authorities, port health authorities and food traders on how to submit a sample for referee analysis.
Check the regulations on aircraft parts imported with a certificate of airworthiness.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
Find registered patents, patent applications and pending patents
A checklist from the Foreign, Commonwealth & Development Office to help British people prepare for travelling and staying safe abroad.
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.
List of Field Safety Notices from 22 to 26 April 2024.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
Pharmacovigilance system requirements
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
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