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How investigators and sponsors should manage clinical trials during COVID-19
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
Placing a veterinary medicine on the market, including non-medicinal products, medicinal words and phrases, how to obtain advice, report non-compliance.
FCDO travel advice for Madagascar. Includes safety and security, insurance, entry requirements and legal differences.
Information for patients, healthcare professionals and developers of new medicines
Alternative Provider Medical Services (Amendment) Directions 2012.
Past and current clinical trials into therapeutic and antiviral treatments for COVID-19, how to take part, and which treatments have proven to be effective.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Information about how to register your homeopathic medicinal product through the Simplified Homeopathic Registration Scheme or the UK Homeopathic National Rules Scheme
Reported problems with the supply of an animal medicine and the date when the issue is expected to be resolved.
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
How to use a cost utility analysis to evaluate your digital health product.
How to use a cost benefit analysis to evaluate your digital health product.
How to use a randomised controlled trial to evaluate your digital health product.
Compare different evaluation approaches and choose an appropriate method.
The committee advises on the safety and quality of herbal medicines when there's an application for registration, marketing authorisation or product licence.
We have more than 10 years’ experience of successfully working with our customers to develop solutions across the radioactive waste lifecycle and provide access to the full range of treatment, logistics, and disposal techniques and technology in the UK, Europe,...
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