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Register to vote Register by 18 June to vote in the General Election on 4 July.
Links to EU guidance, as it stood immediately before end of transition period.
FCDO travel advice for the Turks and Caicos Islands. Includes safety and security, insurance, entry requirements and legal differences.
Guidance for the veterinary pharmaceutical industry on the production and submission of the Summary of Product Characteristics (SPCs) and product literature mock-ups.
This guidance demonstrates stakeholders, including the government, working together to address supply issues.
How investigators and sponsors should manage clinical trials during COVID-19
Helping public health practitioners conducting evaluations – developing a logic model to represent how your intervention works.
How a marketing authorisation holder should report a defect with a veterinary medicine.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Resources to help primary care practitioners promote the appropriate use of antibiotics in dental care.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines in the UK.
This guide is about infections that occur in people who inject drugs (PWID).
Applying for an individual domestic drugs licence to prescribe cocaine, diamorphine and dipipanone for the treatment of addiction.
Information about new applications, post-licensing, advertising, product information and fees.
FCDO travel advice for St Maarten. Includes safety and security, insurance, entry requirements and legal differences.
Ten guiding principles that can inform the development of Good Machine Learning Practice (GMLP).
Information for British people on medical support in Thailand including mental health, lists of hospitals and care homes and how the British embassy can help.
The review of the Committee on Standards in Public Life on the role of leadership in embedding an ethical culture in organisations.
Information about when you need to submit substantial amendments to a clinical trial including changes to the trial sponsor or legal representative, Investigational medicinal product certification and importation.
Urgent safety updates arising from pharmacovigilance data, including reported adverse events, for veterinary medicines authorised in the UK.
Checklists providing a practical guide to using medical devices.
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