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Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
Submission dates and how the submissions using the EC decision reliance procedure work.
Use this form to confirm that your limited liability partnership (LLP) details are up to date.
Information about when you need to submit substantial amendments to a clinical trial including changes to the trial sponsor or legal representative, Investigational medicinal product certification and importation.
Guidance for manufacturers, importers and distributors.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
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
Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
Advice on writing clear notices and maximising replies to your FSNs.
Check the regulations on aircraft parts imported with a certificate of airworthiness.
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.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
Guidance for organisations when making decisions about the design and operation of enterprise IT services which handle OFFICIAL information.
Apply for a higher education course, track your application and accept or reject your offers.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Find registered patents, patent applications and pending patents
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