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Register to vote Register by 18 June to vote in the General Election on 4 July.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
FCDO travel advice for Brazil. Includes safety and security, insurance, entry requirements and legal differences.
Your travel insurance could be invalidated if you travel against advice…
This advice reflects the UK government’s understanding of current rules…
This guide also has safety advice for regions of Brazil. Terrorism There…
This section has safety advice for regions of Brazil. It only covers…
Before you travel check that: your destination can provide the healthcare…
The Foreign, Commonwealth & Development Office (FCDO) cannot provide…
The Medicines and Healthcare products Regulatory Agency regulates medicines, medical devices and blood components for transfusion in the UK. MHRA is an executive agency, sponsored by the Department of Health and Social Care .
FCDO travel advice for Colombia. Includes safety and security, insurance, entry requirements and legal differences.
Reported problems with the supply of an animal medicine and the date when the issue is expected to be resolved.
How we evaluated pre-exposure prophylactic (preventative) treatments for COVID-19.
Information about new applications, post-licensing, advertising, product information and fees.
Information on herbal medicines, how to apply for a traditional herbal registration (THR), banned or restricted herbal ingredients, homeopathic medicines and fees.
FCDO travel advice for Peru. Includes safety and security, insurance, entry requirements and legal differences.
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
How the MHRA makes decisions on what is a medicinal product (borderline products).
For manufacturers and distributors of intermediate and final feedingstuffs containing a medicinal premix or specified feed additives.
There are changes to the legislation of Reference Medicinal Products (RMPs) used to support abridged marketing authorisation applications
Links to EU guidance, as it stood immediately before end of transition period.
The eMIT provides information about prices and usage for generic drugs and pharmaceutical products.
A summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices.
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