MHRA是英国药品监管机构的简称,全称为Medicines and Healthcare products Regulatory Agency,中文为药品和健康产品管理局。MHRA为英国卫生部下属的执行政府机构,保证药物和医疗器械的安全和有效。 本数据库可帮助您快速获知在英国上市药品的最新信息。
QxP said that the MHRA has now received the first deployed VR workstation, which will be upgraded to the full commercial release. The workstation will act as a source of internal training for the MHRA’s GMP Inspectorate, said QxP’s CEO, Crystal Mersh. She said: “We are so pleased to...
The UK MHRA has issued a class 3 drug alert announcing the recall of Scheriproct ointment. Intendis is recalling two batches of its Scheriproct ointment 30g tube. The product contains prednisolone hexanoate and dibucaine [cinchocaine] hydrochloride. Intendis is recalling the batches because of...
CStone Pharmaceuticals announced that the UK Medicines and Healthcare products Regulatory Agency (MHRA) has approved sugemalimab in combination with platinum-based chemotherapy as a first-line treatment for adult patients with metastatic non-small ...
MHRA letter. June 29.2004.Medicines and Healthcare Products Regulatory Agency 105. Martindale's. Pharmacology and Toxicology Center. Prescription & Over-the-Counter Drug Databases:http://www.martindalecenter.com/Pharmacy_6_HuD.html 106. IDIS Ltd. Sourcing Unlicensed Named Patient's Medicines. .http...
The UK’s Medicines and Healthcare Regulatory Agency (MHRA) looks set to take on the responsibilities of the European Medicines Agency (EMA) after that date, and is working through a set of proposals on how to manage functions such as assessing safety and efficacy of drugs. The plans...
What is probably most exciting about ILAP is the bringing together of expertise from the MHRA with that of key HTA agencies NICE and the Scottish Medicines Consortium (SMC), as well as NHS England and NHS Improvement (NHSE&I), and, of course, patients too. It’s the first time that all...
According to press reports, the UK’s drug regulator, the Medicines and Healthcare products Regulatory Authority (MHRA) could become one of the first bodies to approve the vaccine. According to the Financial Times, the MHRA could approve the vaccine by 7th December after the companies announced ...
Last month, the UK Medicines and Healthcare products Regulatory Agency (MHRA) advised against the use of antibody tests based on finger prick blood after several companies started offering this as a service. Like antibody tests developed by AbbVie and Roche, Quotient’s MosaiQ COVID-19 Antibody...
in the European Commission's EU medical device database EUDAMED under a unique Single Registration Number (SRN): XI-AR-000001836 for the markets of EEA/EU27 & Northern Ireland.Wellkang is also a registered UK Responsible Person (UKRP) in the UK MHRA medical device database for the market ...