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How to write requirements for services on the Digital Outcomes and Specialists framework
Guidance on the collection, verification, and reporting of safety events in clinical trials of an investigational medicinal product.
Help your team understand why they need to meet the website and mobile app accessibility regulations.
How to find digital outcome, specialist and user research services on the Digital Outcomes and Specialists framework.
Apply for an authorisation to manufacture extemporaneous preparations, autogenous vaccines, stem cell products or blood products for non-food animals.
The duties and competence requirements for building regulations that clients, designers and contractors must meet.
What you need to do before your product can be placed on the Great Britain market with a UKCA mark.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
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