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How to work out the customs value of imported goods that are free of charge, used, rented or leased if you're an importer or clearing agent.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
We are allowing alternative courses of actions for manufacturing or laboratory equipment during the outbreak.
Guidance for organisations involved in any aspect of the pharmaceutical lifecycle or GLP studies regulated by MHRA, covering the approval of paper documents when working from home
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Information on good laboratory, manufacturing and distribution practice, good pharmacovigilance practice (GPvP), out-of-specification investigations, inspection metrics and fees.
How to use Method 1 to work out the customs value of your imported goods if you're an importer or clearing agent.
How to use a cost utility analysis to evaluate your digital health product.
Emerging techniques on how to prevent or minimise the environmental impacts of post-combustion carbon dioxide capture.
How to use a think aloud study to evaluate your digital health product.
How to use Method 3 to work out the customs value of your imported goods if you’re an importer or clearing agent.
How responders can reduce the risk of communications disruption during emergencies by using ResilienceDirect, HITS and Telecoms Sub-Groups.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
Learn how to check if your website or mobile app is accessible.
How to use routinely collected data to evaluate your digital health product.
Like other forms of property, you can buy, sell and license IP, it is important you understand the value your trade mark, patent or design.
What research and consultancy services Cefas provides, what legislation you need to comply with, and how to meet those requirements.
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