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How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
How to decide what your charity’s purposes are and write them in the ‘objects’ clause of your governing document.
How to use a factorial randomised controlled trial to evaluate your digital health product.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
The Environment Agency’s aims and objectives for Thames Estuary 2100.
This advice summarises the applicant and decision maker obligations under the Habitats Regulations in the context of Nationally Significant Infrastructure Projects (NSIPs).
Find out how the scheme works, including issuing shares and raising money and how to submit a compliance statement.
Actions that trial sponsors should consider to build resilience into clinical trial design
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