MHPRA，全称为Medicines and Healthcare Products Regulatory Agency (MHRA)，是一个在英语中广泛使用的缩写词，中文译为“药品和保健品管理局”。这个机构负责监管药品和保健品的生产和销售，确保公众健康和产品质量。它在英国医学领域具有重要作用，涉及到顺势疗法的审批和对含有声称天然成分的产品进行检查，...
The Medicines and Healthcare products Regulatory Agency regulates medicines, medical devices and blood components for transfusion in the UK. MHRA is an executive agency, sponsored by the Department of Health and Social Care .
Medicines and Healthcare products Regulatory Agency Sort By: Page 1 of 23 - About 226 essays Medical Device Recall: This recall covered two areas: making claims in promotional materials that claims in promotional materials that constitute a medical device but not filing the product as a medical...
网络药物和保健产品监管署;医疗药品暨保健产品管理局;英国药品与保健品管理局 网络释义 1. 药物和保健产品监管署 英国的药品监管机构——药物和保健产品监管署(Medicines and Healthcare Products Regulatory Agency)建议大家不要从网络 … tech.163.com|基于46个网页 ...
药品和健康产品管理局MHRA 药品和健康产品管理局英文简称MHRA,英文全称为Medicines and healthcare products regulatory agency. MHRA为英国卫生部下属的执行政府机构,主管药物和医疗器械的安全和有效,其性质类似于美国FDA或者国内的NMPA 官网:https://www.go
药品和健康产品管理局MHRA 药品和健康产品管理局英文简称MHRA,英文全称为Medicines and healthcare products regulatory agency. MHRA为英国卫生部下属的执行政府机构,主管药物和医疗器械的安全和有效,其性质类似于美国FDA或者国内的NMPA 官网:https://www.go
英语缩写词 "MHRA"，全称为 "Medicines and Healthcare products Regulatory Agency (UK)"，中文直译即为“药品和保健品管理局（英国）”。这个缩写词主要用于表示英国对该领域产品的监管机构，它涵盖了药品和保健品的监管职责。其拼音为 "yào pǐn hé bǎo jiàn pǐn guǎn lǐ jú yīng ...
The Medicines and Healthcare Products Regulatory Agency (MHRA) is the government agency that regulates pharmaceuticals, blood establishments, advanced therapy medical products, and medical devices in the United Kingdom. Working under the Department of Health, the MHRA also incorporates the National ...
Chapter 1 - Medicines and Healthcare products Regulatory Agency 热度: Glucose PL 00116-0406 - Medicines and Healthcare products :葡萄糖PL 00116-0406 -药物及保健产品 热度: building parity between brand and generic peptide products regulatory and scientific considerations for quality of synth.之间建立平...
Medicines and Healthcare products Regulatory Agency (UK). MDA/2003/001 - Reporting Adverse Incidents & Disseminating Medical Device Alerts. London, Medicines and Healthcare products Regulatory Agency, 2003.Medicines and Healthcare products Regulatory Agency (MHRA) [internet]. Minutes of the meeting of...