In a UK-first, the Medicines and Healthcare products Regulatory Agency (MHRA) and Barts Health NHS Trust have developed a DNA sequencing approach that can be...

The MHRA products website allows you to find: The leaflets which are provided with medicines; The description of the medicinal product’s properties and how it can be used; Scientific reports...

Manufacturers, importers and distributors of active substances are required to register their activities with the MHRA. Since inspections of manufacturers of active substances are based on risk,...

We are the regulator of medicines, medical devices and blood components for transfusion in the UK. We put patients first in everything we do, right across the lifecycle of the products we regulate.

The MHRA is an executive agency sponsored by the Department of Health and Social Care which regulates medicines, medical devices and blood components for transfusion in the UK. The MHRA has been actively involved in the Vaccine Taskforce and is responsible for regulatory oversight of vaccine manufacture.

MHRA-GMDP contains information relating to manufacturing and wholesale distribution authorisations, API registrations and GMP/GDP certificates.

2024年12月25日 · 英国药品与医疗保健产品监管机构（Medicines and Healthcare products Regulatory Agency，MHRA）提供了一个产品网站，允许用户查找任何单词、短语或产品许可证号码（PL）。可以通过搜索工具搜索，或者使用A-Z列表来查找药品信息。 查询网址：https://products.mhra.gov.uk/

2014年5月28日 · Queries on registering and submitting product licence applications using the MHRA Portal, phone: 020 3080 7100 or email [email protected]. MHRA Submissions Portal Guidance:...

MHRA全称Medicinesand Healthcare products Regulatory Agency，负责监管英国医疗器械市场，对英国设备的市场营销和供应做出决定。并负责指定和监督英国合格评定机构。本文将对MHRA注册和UKCA实施简单说明，一起了…

2023年12月11日 · GMP and GCP Inspectors work closely with MHRA Clinical Trials and regularly provide support to help answer a wide range of stakeholder queries which relate to the manufacture, import, labelling,...