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How investigators and sponsors should manage clinical trials during COVID-19
Information for prospective growers of low THC cannabis (industrial hemp), for the production of seed and fibre only.
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.
When to book your motorcycle theory test, what to take with you, how the multiple-choice questions and hazard perception test work, and the pass mark
When entering the UK, you need to prove your medicine is prescribed to you if it contains a controlled drug - find out what proof you need to get.
Information for British nationals who have been affected by rape or sexual assault abroad, including how to contact the Foreign, Commonwealth & Development Office, and how to access medical attention and legal advice when returning to the UK.
How to account for VAT if you make supplies to your customers, and you pay certain costs that you pass on when you invoice them.
How to get a parallel import licence for your medicine in the UK, including pharmacovigilance requirements and submitting your application.
From next month women in England can get their contraceptive pills without contacting their GP first.
Guidance for people with symptoms of a respiratory infection including COVID-19, or a positive test result for COVID-19.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Advice for medical professionals to follow when assessing drivers with neurological disorders.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
What you need to know and do before you book any travel to the UK.
FCDO travel advice for Guatemala. Includes safety and security, insurance, entry requirements and legal differences.
These reports explain our assessment of the scientific evidence used to lead to regulatory decisions on the safety of medicines or medicines classes.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Advice for medical professionals to follow when assessing drivers with diabetes mellitus.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
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