BS DD ISO TS 25237-2009 Health informatics - Pseudonymization《健康信息 Pseudonymization》.pdf
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1、DD ISO/TS25237:2008ICS 35.240.80NO COPYING WITHOUT BSI PERMISSION EXCEPT AS PERMITTED BY COPYRIGHT LAWDRAFT FOR DEVELOPMENTHealth informatics PseudonymizationThis Draft for Developmentwas published under theauthority of the StandardsPolicy and StrategyCommittee on 31 January2009 BSI 200ISBN 978 0 58
2、0 64750 5Amendments/corrigenda issued since publicationDate CommentsDD ISO/TS 25237:2008National forewordThis Draft for Development is the UK implementation of ISO/TS25237:2008.This publication is not to be regarded as a British Standard.It is being issued in the Draft for Development series of publ
3、ications andis of a provisional nature. It should be applied on this provisional basis,so that information and experience of its practical application can beobtained.Comments arising from the use of this Draft for Development arerequested so that UK experience can be reported to the internationalorg
4、anization responsible for its conversion to an international standard.A review of this publication will be initiated not later than 3 years afterits publication by the international organization so that a decision can betaken on its status. Notification of the start of the review period will bemade
5、in an announcement in the appropriate issue of Update Standards.According to the replies received by the end of the review period,the responsible BSI Committee will decide whether to support theconversion into an international Standard, to extend the life of theTechnical Specification or to withdraw
6、 it. Comments should be sent tothe Secretary of the responsible BSI Technical Committee at BritishStandards House, 389 Chiswick High Road, London W4 4AL.The UK participation in its preparation was entrusted to TechnicalCommittee IST/35, Health informatics.A list of organizations represented on this
7、committee can be obtained onrequest to its secretary.This publication does not purport to include all the necessary provisionsof a contract. Users are responsible for its correct application.Compliance with a British Standard cannot confer immunityfrom legal obligations.9DD ISO/TS 25237:2008Referenc
8、e numberISO/TS 25237:2008(E)ISO 2008TECHNICAL SPECIFICATION ISO/TS25237First edition2008-12-01Health informatics Pseudonymization Informatique de sant Pseudonymisation DD ISO/TS 25237:2008ISO/TS 25237:2008(E) PDF disclaimer This PDF file may contain embedded typefaces. In accordance with Adobes lice
9、nsing policy, this file may be printed or viewed but shall not be edited unless the typefaces which are embedded are licensed to and installed on the computer performing the editing. In downloading this file, parties accept therein the responsibility of not infringing Adobes licensing policy. The IS
10、O Central Secretariat accepts no liability in this area. Adobe is a trademark of Adobe Systems Incorporated. Details of the software products used to create this PDF file can be found in the General Info relative to the file; the PDF-creation parameters were optimised for printing. Every care has be
11、en taken to ensure that the file is suitable for use by ISO member bodies. In the unlikely event that a problem relating to it is found, please inform the Central Secretariat at the address given below. COPYRIGHT PROTECTED DOCUMENT ISO 2008 All rights reserved. Unless otherwise specified, no part of
12、 this publication may be reproduced or utilised in any form or by any means, electronic or mechanical, including photocopying and microfilm, without permission in writing from either ISO at the address below or ISOs member body in the country of the requester. ISO copyright office Case postale 56 CH
13、-1211 Geneva 20 Tel. + 41 22 749 01 11 Fax + 41 22 749 09 47 E-mail copyrightiso.org Web www.iso.org Published in Switzerland ii ISO 2008 All rights reservedDD ISO/TS 25237:2008ISO/TS 25237:2008(E) ISO 2008 All rights reserved iiiContents Page Foreword iv Introduction v 1 Scope . 1 2 Normative refer
14、ences . 1 3 Terms and definitions. 1 4 Symbols (and abbreviated terms) . 6 5 Requirements for privacy protection of identities in healthcare . 6 5.1 A conceptual model for pseudonymization of personal data 6 5.2 Categories of data subject. 13 5.3 Classification of data 14 5.4 Trusted services . 16 5
15、.5 Need for re-identification of pseudonymized data 16 5.6 Pseudonymization service characteristics 17 6 Pseudonymization process (methods and implementation) 18 6.1 Design criteria . 18 6.2 Entities in the model. 18 6.3 Workflow in the model 20 6.4 Preparation of data . 21 6.5 Processing steps in t
16、he workflow. 22 6.6 Protecting privacy protection through pseudonymization 23 7 Re-identification process (methods and implementation) . 27 8 Specification of interoperability of interfaces (methods and implementation) 28 9 Policy framework for operation of pseudonymization services (methods and imp
17、lementation) 29 9.1 General. 29 9.2 Privacy policy 29 9.3 Trustworthy practices for operations. 30 9.4 Implementation of trustworthy practices for re-identification . 31 Annex A (informative) Healthcare pseudonymization scenarios 33 Annex B (informative) Requirements for privacy risk assessment desi
18、gn 46 Bibliography . 56 DD ISO/TS 25237:2008ISO/TS 25237:2008(E) iv ISO 2008 All rights reservedForeword ISO (the International Organization for Standardization) is a worldwide federation of national standards bodies (ISO member bodies). The work of preparing International Standards is normally carr
19、ied out through ISO technical committees. Each member body interested in a subject for which a technical committee has been established has the right to be represented on that committee. International organizations, governmental and non-governmental, in liaison with ISO, also take part in the work.
20、ISO collaborates closely with the International Electrotechnical Commission (IEC) on all matters of electrotechnical standardization. International Standards are drafted in accordance with the rules given in the ISO/IEC Directives, Part 2. The main task of technical committees is to prepare Internat
21、ional Standards. Draft International Standards adopted by the technical committees are circulated to the member bodies for voting. Publication as an International Standard requires approval by at least 75 % of the member bodies casting a vote. In other circumstances, particularly when there is an ur
22、gent market requirement for such documents, a technical committee may decide to publish other types of document: an ISO Publicly Available Specification (ISO/PAS) represents an agreement between technical experts in an ISO working group and is accepted for publication if it is approved by more than
23、50 % of the members of the parent committee casting a vote; an ISO Technical Specification (ISO/TS) represents an agreement between the members of a technical committee and is accepted for publication if it is approved by 2/3 of the members of the committee casting a vote. An ISO/PAS or ISO/TS is re
24、viewed after three years in order to decide whether it will be confirmed for a further three years, revised to become an International Standard, or withdrawn. If the ISO/PAS or ISO/TS is confirmed, it is reviewed again after a further three years, at which time it must either be transformed into an
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