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Descriptions of team capabilities on the Digital Outcomes and Specialists framework.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
What blood establishments, blood banks and manufacturers of blood products need to do to ensure the safety and quality of blood and blood products.
How to use a cost benefit analysis to evaluate your digital health product.
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.
Information on OPSS product safety alerts, reports and recalls for unsafe products and resources for consumers, businesses and regulators.
You can only import certain goods using an ATA Carnet to claim relief under temporary admission in the UK. Some goods have special conditions attached.
Qualified Persons (QPs) should follow the below guidance on the flexible approaches we are taking for medicines imported from third countries.
Information about how to register your homeopathic medicinal product through the Simplified Homeopathic Registration Scheme or the UK Homeopathic National Rules Scheme
A complete list of 5G projects involved in the 5G Testbeds and Trials Programme
Licences and authorisations to import genetic material, research and diagnostic samples, trade samples and display items, and some live animals and animal products.
Find out about the rules for placing transportable pressure equipment on the market in Great Britain from 1 January 2023.
Get endorsement for the Global Talent visa to work in the UK as a digital technology expert - fintech, gaming, cyber security, artificial intelligence
Check what you need to do to sell cosmetic products in Great Britain.
Comply with good pharmacovigilance practice and prepare for an inspection.
Explore a system as a user would - without a script or set of tasks - to find possible defects that other forms of testing may miss.
Guidance for local authorities, port health authorities and food traders on how to submit a sample for referee analysis.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
DNA testing can be used in child maintenance or inheritance disputes, or applications for contact with a child or for a child to settle in the UK
Actions that trial sponsors should consider to build resilience into clinical trial design
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