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Helping public health practitioners conducting evaluations – developing a logic model to represent how your intervention works.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Project Orbis is a programme to review and approve promising cancer drugs helping patients access treatments faster.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Find out if you need to apply for the fit and proper test and how to do this so that HMRC can register your business.
This guidance explains what rules of origin (RoOs) are and the changes under the Developing Countries Trading Scheme (DCTS).
Information on UK sanctions currently in place and how to apply for the appropriate licences.
Read the Council Directive 2003/48/EC of 3 June 2003 on taxation of savings income in the form of interest payments.
How to use a before-and-after study to evaluate your digital health product.
How to use an N-of-1 study to evaluate your digital health product.
Helping public health practitioners conducting evaluations – using outcome evaluations to find out if an intervention works.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Licensing bodies and collective management organisations can agree licences with users on behalf of owners and collect any royalties the owners are owed.
Find out about the Industry Security Assurance Centre (ISAC) and its associated responsibilities.
Responding to suspected breaches of planning control.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
How to use an economic evaluation to evaluate your digital health product.
How to apply for the different simplified declarations for exports and what you need for authorisation to use them.
How the MHRA processes variations to Marketing Authorisations (MAs)
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
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