Medicines and Healthcare products Regulatory Agency (MHRA) of United Kingdom

The Medicines and Healthcare products Regulatory Agency (MHRA) is a key authority in the United Kingdom that ensures the safety and effectiveness of medicines and medical devices. It regulates healthcare products, monitors their use, and provides clear guidance to protect public health.

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Suspended and Revoked Manufacturing and Wholesale Distribution Authorisations by MHRA

This page provides a comprehensive list of Manufacturing and Wholesale Distribution authorisations that have been suspended or revoked by the Medicines and Healthcare products Regulatory Agency (MHRA). These actions are taken to ensure public safety and maintain the integrity of the UK’s healthcare system.
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FAQs

Why is compliance with the Medicines and Healthcare products Regulatory Agency (MHRA) of United Kingdom necessary?

Compliance with the Medicines and Healthcare Products Regulatory Agency (MHRA) regulations is essential to ensure the safety and efficacy of medical products in the United Kingdom. Adhering to these guidelines protects public health by preventing the release of substandard or unsafe medicines and healthcare products. Additionally, compliance fosters trust among healthcare professionals and patients, ensuring that products meet rigorous quality standards. Non-compliance can lead to legal repercussions, financial penalties, and damage to a company’s reputation, making adherence vital for sustained operations.

Which companies should comply with Medicines and Healthcare products Regulatory Agency (MHRA) of United Kingdom?

The Medicines and Healthcare Products Regulatory Agency (MHRA) oversees compliance for pharmaceutical and healthcare companies in the UK. This includes manufacturers, importers, and distributors of medicines, medical devices, and clinical trial sponsors. Compliance is crucial to ensure product safety, efficacy, and quality, safeguarding public health while also meeting legal obligations to avoid severe penalties and maintain market access.