Vigilance or other Medical Device Adverse Event Reporting选择语言:从 到 翻译结果1翻译结果2 翻译结果3翻译结果4翻译结果5 翻译结果1复制译文编辑译文朗读译文返回顶部 警惕或其他医疗器械不良事件报告 翻译结果2复制译文编辑译文朗读译文返回顶部 警惕或者其他医学设备不利的事件报告 翻译结果3复制译文编辑译文朗读...
Disclosed are techniques for predicting, reporting, and preventing medical adverse events, such as septicemia. The techniques may be implemented in a client-server arrangement, where the clients are present on medical professionals' smart phone, for example. The disclosed techniques' ability to detect...
Four sets of IMDRF Adverse Event Reporting terminology and aligned documentaries: (1) Medical device problem terminology, (2) components terminology, (3) cause investigation terminology and (4) patient problem terminology. Modified from “The advesre event reporting terminology is composed of four set...
FORHEALTHCAREPROFESSIONALSREPORTINGMEDICALDEVICEADVERSEEVENTSHowtosubmityourmedicaldeviceadverseevent(AE)report?YoucanreportallsuspectedmedicaldeviceAEtoHSAatTel:68663538Fax:64789069Email:HSA_productsa ety@hsa.gov.sgAllreporting ormsareavailableat:http://.hsa.gov.sg/publish/hsaportal/en/health_products_regulati...
On November 27, 2020, the National Medical Products Administration (NMPA) issued (No.78 – 2020) the guideline for the standard procedure that NMPA Legal Agents shall follow when submitting risk evaluation reports after an adverse event. In general, the medical device registrants or filing person...
2.The reporting of medical device adverse event(MDAE) is the first step on the detection of medical device problems and taking risk management actions.医疗器械不良事件报告是发现医疗器械安全性隐患和采取风险管理措施的前提。 英文短句/例句 1.Study on Training Needs for Survey of Adverse Effects of ...
In view of the medical device adverse event reports the status quo, explore the impact of medical device adverse event reporting factors, summarized the limitations of their conduct in 翻译结果3复制译文编辑译文朗读译文返回顶部 Status of Chinese medical device adverse event reports, discussion on the...
Aversionofthisreportwaspublishedas“ReportingAdverseDrugandMedicalDeviceEvents”FoodandDrugLawJournal.1994;49(2):359-366.©1993–1994AmericanMedicalAssociation.AllRightsReserved.CEJAReportB–A-93ReportingAdverseDrugandMedicalDeviceEventsBACKGROUNDINFORMATIONANDIMPORTANCEOFREPORTINGTheFoodandDrugAdministration(FDA)oper...
Medical device reporting (MDR) software is designed for medical device companies to manage reporting processes.
aThe purpose of this document is to describe the procedure to be followed for implementing the Adverse Event Reporting or Medical Device Reporting Event (MDR) regulations of the Food and Drug Administration under 21 CFR 803. ... 正在翻译,请等待...[translate]...