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How investigators and sponsors should manage clinical trials during COVID-19
Tell users how accessible your website or mobile app is in your accessibility statement, based on recent testing.
Find out how to import your personal belongings, pets and private motor vehicles when moving or returning to the UK.
Configure email services securely using encryption and anti-spoofing.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
A guide to collecting data about your packaging. This is for UK organisations affected by extended producer responsibility (EPR) for packaging.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Biosecurity and hygiene standards to keep birds safe from bird flu (avian influenza).
What to do if you think you are a victim of identity theft or fraud, and what signs to look out for.
Information and guidance on a range of medical devices for users and patients.
The information that schools maintained by their local authorities must or should publish on their websites.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Pharmacovigilance system requirements
Find out how to prove the originating status of your goods and check if you can claim preferential tariff treatment.
Guidance and advice for candidates using the Civil Service Jobs website.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
How to use a before-and-after study to evaluate your digital health product.
A checklist from the Foreign, Commonwealth & Development Office to help British people prepare for travelling and staying safe abroad.
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