scholarly journals Necessary Processing of Personal Data: The Need-to-Know Principle and Processing Data from the New German Identity Card

Author(s):  
Harald Zwingelberg
2012 ◽  
Vol 45 (6) ◽  
pp. 1697-1701 ◽  
Author(s):  
A. Cernian ◽  
A. Olteanu ◽  
G. Mateescu ◽  
M. Vladescu ◽  
Gr. Stamatescu ◽  
...  

Author(s):  
Jens Bender ◽  
Özgür Dagdelen ◽  
Marc Fischlin ◽  
Dennis Kügler

2015 ◽  
Vol 3 (1) ◽  
Author(s):  
Shony Mathew P. J ◽  
Dr. Vidhya Ravindranadan

Vocational Rehabilitation is the part of continuous and coordinated process of rehabilitation which involves the guidance, vocational training and selective placement designed to enable a differently abled person to secure and retain suitable employment. The present study analyzes impact of vocational training in the competencies of mild mentally challenged adults. The sample for the study consists of 8 mild mentally challenged adults between the age of 18 -30 years. An individualized vocational curriculum is developed and the vocational training courses provided training in computer, stitching, embroidery, office assistance and identity card making. Pre test-post test design has been used in order to understand the influence of intervention. For this purpose Behavioral Assessment Scales for Adult Living – Mental Retardation (BASAL –MR) and Personal data sheet has been used. The results indicate that vocational training has great impact in developing competencies of mild mentally challenged.


Author(s):  
Olexander Zadereyko ◽  
Olena Trofymenko ◽  
Nataliia Loginova

In the European Union, in the first half of 2018, the General Data Protection Regulation came into force, which established the new rules for processing users’ personal data for IT companies. The operating systems (OS) are the dominant software that is responsible for collecting and processing data in computer systems. The most common OS is the Windows OS family. The authors identified Windows 10 operating systems, that collect and accumulate user's personal data; developed and tested practically an algorithm, the application of which localizes and blocks the transfer of user's personal data to official servers of the Microsoft company.


2019 ◽  
Vol 29 (5) ◽  
pp. 34-37
Author(s):  
Suzanne Lurie

This article examiness the lawful bases for processing data under GDPR, why consent is not an appropriate lawful basis and which lawful basis a clinician should rely on for the processing of personal data


2005 ◽  
Vol 12 (4) ◽  
pp. 357-372 ◽  
Author(s):  
Asim Sheikh

AbstractDirective 95/46/EC on the Protection of Individuals with regard to the Processing of Personal Data and on the Free Movement of Such Data has been transposed into national law and is now the Data Protection (Amendment) Act, 2003.The Directive and the transposing Act provide for new obligations to those processing data. The new obligation of primary concern is the necessity to obtain consent prior to the processing of data (Article 7, Directive 95/46/EC). This has caused much concern especially in relation to 'secondary data' or 'archived data'.There exist, what seem to be in the minds of the medical research community, two competing interests: (i) that of the need to obtain consent prior to processing data and (ii) the need to protect and foster medical research. At the same time as the introduction of the Act, other prior legislation, i.e. the Freedom of Information Act, 1997-2003, has encouraged candour within the doctor-patient relationship and the High Court in Ireland, in the case of Geoghegan v. Harris, has promulgated the 'reasonable-patient test' as being the correct law in relation to the disclosure of risks to patients. The court stated that doctors have a duty to disclose all material risks to patients. The case demonstrates an example of a move toward a more open medical relationship. An example of this rationale was also recently seen in the United Kingdom in the House of Lords decision in Chester v. Afshar. Within the medical research community in Ireland, the need to respect the autonomy of patients and research participants by providing information to such parties has also been observed (Sheikh A. A., 2000 and Irish Council for Bioethics, 2005).Disquiet has been expressed in Ireland and other jurisdictions by the medical research communities in relation to the exact working and meaning of the Directive and therefore the transposing Acts (Strobl et al). This may be due to the fact that, as observed by Beyleveld "The Directive makes no specific mention of medical research and, consequently, it contains no provisions for medical research as an explicitly delineated category." (Beyleveld D., 2004) This paper examines the Irish Act and discusses whether the concerns expressed are well-founded and if the Act is open to interpretation such that it would not hamper medical research and public health work.


1971 ◽  
Vol 10 (03) ◽  
pp. 142-147
Author(s):  
M. RENAUD ◽  
M. AQARQ ◽  
R. GERARD-MARCHANT ◽  
M. WOLFF-TERROINE

A method is presented for processing data from the histopathological laboratory of a cancer hospital. Emphasis is laid on the ease of use, the connection of medical, administrative and financial data, and the strictness of control of patient’s identification number. The system can be used separately; it is also a module for a large integrated system covering all the activities of the hospital.


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