Medical Device Regulatory Data Online—Part 3

Bonnie Snow

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Medical Device Regulatory Data Online—Part 3

机译：在线医疗设备监管数据-第3部分

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Monitoring U.S. Pood and Drug Administration activities is important to both business and bio-medical researchers. As the primary gatekeeper to the lucrative drug and medical technology marketplace, the FDA's decisions regarding new therapeutic product introductions affect an incredibly broad range of interrelated commercial enterprises, including not only prospective buyers, insurers and investors, but also advertising agencies, legal counsel, shipping companies, packaging firms, etc. Knowing where and how to search for documents related to this federal agency's actions has been the subject of several Caduceus installments since the column began in 1985.

机译：监视美国Pood和药物管理局的活动对商业和生物医学研究人员都很重要。作为进入利润丰厚的药物和医疗技术市场的主要守门人，FDA关于引入新治疗产品的决定影响到范围广泛的相互关联的商业企业，不仅包括准买家，保险人和投资者，还包括广告代理商，法律顾问，运输自从该专栏于1985年开始以来，知道如何在何处以及如何搜索与该联邦机构行动有关的文件一直是Caduceus分期付款的主题。

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《Database》 |1995年第3期|p.98-100102-103|共5页
作者
Bonnie Snow;
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正文语种 eng
中图分类计算机软件;
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1. Medical Device Regulatory Data Online—Part 2 [J] . Bonnie Snow Database . 1995,第2期

机译：在线医疗设备监管数据-第2部分
2. Tracking Down Medical Device Regulatory Data Online [J] . Bonnie Snow Database . 1995,第1期

机译：在线追踪医疗设备监管数据
3. Medical devices. Regulatory framework and contribution of the German Federal Institute for Drugs and Medical Devices (Bf ArM) to the safe application [J] . Wolfgang Lauer, E. StoBlein, A. Brinker, Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz . 2014,第12期

机译：医疗设备。德国联邦药品和医疗器械研究所（Bf ArM）的法规框架和对安全应用的贡献
4. CARDIOVASCULAR MEDICAL DEVICES: REGULATORY SCIENCE RESEARCH OVERVIEW IN THE OFFICE OF SCIENCE AND ENGINEERING LABORATORIES (OSEL) AT THE FOOD AND DRUG ADMINISTRATION (FDA) [C] . Kenneth Aycock, Ksenia Blinova, Maura Casciola, Design of Medical Devices Conference . 2021

机译：心血管医疗器械：监管科学研究概述在食品和药物管理局（FDA）的科学与工程实验室（OSEL）办公室
5. An analysis of third-party regulatory audit systems for medical device safety. [D] . Gill, Lillian J. 2004

机译：对医疗器械安全性第三方监管审核系统的分析。
6. The state of artificial intelligence-based FDA-approved medical devices and algorithms: an online database [O] . Stan Benjamens, Pranavsingh Dhunnoo, Bertalan Meskó 2020

机译：基于人工智能的FDA批准的医疗设备和算法的状态：在线数据库
7. Changes in the Medical Device’s Regulatory Framework and Its Impact on the Medical Device’s Industry: From the Medical Device Directives to the Medical Device Regulations [O] . Magali Contardi 2019

机译：医疗设备监管框架的变化及其对医疗器械行业的影响：从医疗器械指令到医疗器械规定
8. Regulatory Responsibilities of the Bureau of Medical Devices. Module V: Overview of the Medical Device Amendments. Leader Guide and Student Workbook [R] . 1980

机译：医疗器械局的监管责任。第五单元：医疗器械修正案概述。领导指南和学生作业簿

Medical Device Regulatory Data Online—Part 3

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