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Data, Freedom of Information releases and corporate reports
Information on the reporting, investigation and management of acute flaccid paralysis (AFP) and acute flaccid myelitis (AFM).
The MHRA is ready to provide any assistance for clinical trials applications submitted for COVID-19
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
FCDO travel advice for Guatemala. Includes safety and security, insurance, entry requirements and legal differences.
The characteristics, diagnosis, management, surveillance and epidemiology of Staphylococcus aureus.
UK Health Security Agency (UKHSA) prevents, prepares for and responds to infectious diseases, and environmental hazards, to keep all our communities safe, save lives and protect livelihoods. We provide scientific and operational leadership, working with local, national and international partners...
The CMA has accepted commitments offered by Google that address the CMA’s competition concerns resulting from investigating Google’s proposals to remove third-party cookies and other functionalities from its Chrome browser.
This guidance specifies the standards for the continuous monitoring and sampling of stack emissions.
Guidance and support on coronavirus (COVID-19) in Scotland.
Data on the real-world efficacy of the COVID-19 vaccines.
Providing vital research into COVID-19 immunity and vaccine effectiveness nationally.
Blogs where government organisations talk about their work and share information and ideas.
Advice and guidance on the health needs of migrant patients from Uruguay for healthcare practitioners.
The Defence and Security Accelerator (DASA) finds and funds exploitable innovation for a safer future. DASA is part of the Ministry of Defence .
Guidance for the veterinary pharmaceutical industry on the production and submission of the Summary of Product Characteristics (SPCs) and product literature mock-ups.
Browse cases data for specific areas within the UK.
How marketing authorisation holders should inform MHRA of a signal or an ADR to a medicine.
These reports explain our assessment of the scientific evidence used to lead to regulatory decisions on the safety of medicines or medicines classes.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
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