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Health issues associated with vulnerability to poor solid waste management, especially among workers directly exposed to these wastes to these wastes.
How to begin with evaluating a digital health product, including when to evaluate, budgeting and getting support.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
As part of Dstl's commitment to improving access to technologies, we're making some of our intellectual property (IP) available for free.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
How to account for VAT on goods and services provided by registered health professionals, including doctors, dentists, nurses and pharmacists.
Applications received to amend the specification of a patent under sections 27 and 75 before the court and the Office.
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
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