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Information to support your recovery after COVID-19.
Guidance and support on coronavirus (COVID-19) in Wales.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Blogs where government organisations talk about their work and share information and ideas.
How to do a Getein Biotech rapid nose-only test for COVID-19. Rapid tests show the result on a device that comes with the test.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
How to conform with the legal requirements for placing medical devices on the market.
Advice on writing clear notices and maximising replies to your FSNs.
How to use a case-control study to evaluate your digital health product.
Apply for a higher education course, track your application and accept or reject your offers.
Find registered patents, patent applications and pending patents
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.
Get information on teacher training courses, funding, pay scales and how to make a great application
Advice and guidance on the health needs of migrant patients from Argentina for healthcare practitioners.
Check the regulations on aircraft parts imported with a certificate of airworthiness.
Pharmacovigilance system requirements
Information about the EU Regulations and their implementation in Northern Ireland
Covering thalidomide, lenalidomide, and pomalidomide: temporary guidance for pregnancy prevention arrangements for patients taking them during COVID-19
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