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欧洲健康数据保护立法建议。

Recommendations for European health data protection legislation.

作者信息

Callens S, Nys H

机构信息

Katholieke Universiteit Leuven, Faculteit Geneeskunde, Centrum voor BioMedische Ethiek en Recht, Belgium.

出版信息

Stud Health Technol Inform. 1996;27:23-52.

Abstract

In year 1 of the SEISMED project, the Katholieke Universiteit Leuven coordinated the inventory and analysis of medical personal data protection legislation in Europe. A report on legal issues of medical data protection legislation in Europe was written by the Vrije Universiteit Amsterdam, the Centre National pour la Recherche Scientifique (Paris) and the University College Dublin. This report served as a basis for a second important legal deliverable, i.e. the Health Informatics Deontology Code. In this third and final report, we take into account the results of the other two legal reports and we formulate recommendations for the national and European legislator. This report analyses critically the upcoming privacy directive. We propose several recommendations which should be taken into account by the European and national legislator. We focused quite extensively on the use of medical data for research purposes. We had several reasons to do this. One of them is the fact that the use of medical data for research purposes is very popular, in particular now the health care sector is becoming more and more 'standardized' by using computers, networksystems and telematics. Legislation is therefore needed. Moreover, the use of medical data for research purposes involves the transfer of data from one Member State to another. Therefore, a harmonized legislation is really needed. We hope that the recommendations we propose, will be taken into consideration by the European legislator.

摘要

在SEISMED项目的第一年,鲁汶天主教大学负责协调对欧洲医疗个人数据保护立法的清查与分析。关于欧洲医疗数据保护立法法律问题的一份报告由阿姆斯特丹自由大学、法国国家科学研究中心(巴黎)和都柏林大学学院撰写。该报告成为第二项重要法律成果——《健康信息学道义准则》的基础。在这份第三份也是最后一份报告中,我们考虑了其他两份法律报告的结果,并为国家和欧洲立法者制定了建议。本报告对即将出台的隐私指令进行了批判性分析。我们提出了若干建议,欧洲和国家立法者应予以考虑。我们相当广泛地关注了医学数据在研究目的方面的使用。我们这样做有几个原因。其中之一是,将医学数据用于研究目的非常普遍,尤其是现在医疗保健部门通过使用计算机、网络系统和远程信息处理技术变得越来越“标准化”。因此需要立法。此外,将医学数据用于研究目的涉及数据从一个成员国向另一个成员国的转移。因此,确实需要统一的立法。我们希望我们提出的建议能得到欧洲立法者的考虑。

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