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Departments, agencies and public bodies
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Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
How to take part in user research at the UK IPO – signing up, who we want to meet with, why we research and your data rights.
You can claim relief to pay no Customs Duty and VAT if you're importing therapeutic substances of human origin, blood-grouping or tissue-typing reagents, or related packaging, solvents and accessories.
Common user charge rates and how the charge applies to imports entering Great Britain through the Port of Dover and Eurotunnel.
Structuring, designing and publishing your API documentation
Guidance to hospital blood banks (HBBs) on flexible approaches to requirements
Information about licences, regulations and safety related to human blood and blood products, including blood and tissue donations from the human body.
The Authority was responsible for organising the donation of blood and preparing it for use by health services. The Authority was abolished in 2005 with responsibilities passing to the NHS Blood and Transplant Service.
TACO is one of the most common causes of transfusion-related deaths in the UK and cases have increased substantially in recent years. Identifying risk factors for TACO prior to transfusion allows initiation of appropriate mitigating measures.
This guide is about infections that occur in people who inject drugs (PWID).
This strategy sets out how DWP intends to increase the quantity and quality of user engagement with the National and Official Statistics it produces.
Information for healthcare professionals on how pulse oximeters are regulated, home use and issues to look out for when using the devices
The Brucella Reference Unit (BRU) provides laboratory diagnostic and clinical management services for Brucella species.
You may need to tell DVLA if you have high or low blood pressure - download form to inform DVLA
What users need to know to know about the Taking Part survey.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
The Medicines and Healthcare products Regulatory Agency (MHRA) has today (11 March 2024) approved the medicine quizartinib (Vanflyta) to be used alongside chemotherapy as first line treatment for adults who have acute myeloid leukaemia (AML).
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Form (S41) for requesting adenovirus testing in whole blood by the blood borne virus unit (BBVU).
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