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Intellectual property can be bought, sold or licensed.
Find out what compound products are, and how to import or move them from the EU to Great Britain.
Find out the rules to establish the country of origin of imported and exported goods and to help identify goods which qualify for lower or no Customs Duty.
How to use a combination of quantitative and qualitative data to evaluate your digital health product.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Food and drink labelling and packaging regulations - what you must show, warnings, health and organic labels and packaging standards.
This guidance explains what rules of origin (RoOs) are and the changes under the Developing Countries Trading Scheme (DCTS).
Compare different evaluation approaches and choose an appropriate method.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to use a before-and-after study to evaluate your digital health product.
There are changes to the legislation of Reference Medicinal Products (RMPs) used to support abridged marketing authorisation applications
Find out if you will need to use the new UKNI marking and how to use it.
What intellectual property is, how you can protect it, and which of copyright, patents, design right and trade marks applies to your work
Guidance for suppliers and dealers.
Apply for an authorisation to manufacture authorised veterinary medicines and medicines marketed under the Exemptions for Small Pet Animals.
Information for manufacturers.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
How to use a cost utility analysis to evaluate your digital health product.
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