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Patient safety

Guidance and regulation

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  • Guidance for healthcare professionals about safeguarding vulnerable individuals from being drawn into terrorism.

  • Information about how to register your homeopathic medicinal product through the Simplified Homeopathic Registration Scheme or the UK Homeopathic National Rules Scheme

  • Guidance for importers of unlicensed human medicines on meeting the requirements of the TSE (Transmissible Spongiform Encephalopathies) guidelines.

  • This action plan sets out the measures that will be used to make NHS maternity services safer.

  • Guidance for healthcare professionals on effectively decontaminating endoscopes.

  • Sets out the progress made in applying the lessons learned from the failings at Mid Staffordshire NHS Foundation Trust.

  • How to use RamaXL, including system availability, running reports and how to subscribe.

  • Current listing of UK brokers authorised to broker human medicines, including company name, registration and address.

  • The Thirlwall Inquiry has been set up to examine events at the Countess of Chester Hospital and their implications following the trial, and subsequent convictions, of former neonatal nurse Lucy Letby of murder and attempted …

  • An overview of the legal requirements for children’s medicines that Marketing Authorisation Holders (MAHs) need to abide by.

  • Some of the different symbols used on medical devices.

  • Information on the safety of transplanting human organs, tissues and cells from the advisory committee on the Safety of Blood, Tissues and Organs (SaBTO).

  • Guidance for safe use in medical, surgical, dental and aesthetic practices

  • E-learning modules for healthcare professionals on minimising the risks of using medicines and information on how to access medical device modules.

  • Guidance for healthcare professionals about how to share information to safeguard individuals from radicalisation.

  • Sets out legal responsibilities for the management of information in NHS organisations.

  • NHS prostate cancer risk management programme (PCRMP) guidance on performing an ultrasound-guided prostate biopsy.

  • Guidance on naming human medicines, including Braille requirements for the name on the product label.

  • Record retention and disposal policy.

  • Cancel a marketing authorisation, traditional herbal registration or parallel import product licence or withdraw a pending submission.