EN ISO 25237-2017 en Health informatics - Pseudonymization《健康信息学pseudonymization(ISO 25237 2017)》.pdf
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1、BS EN ISO 25237:2017Health informatics Pseudonymization (ISO25237:2017)BSI Standards PublicationWB11885_BSI_StandardCovs_2013_AW.indd 1 15/05/2013 15:06BS EN ISO 25237:2017 BRITISH STANDARDNational forewordThis British Standard is the UK implementation of EN ISO 25237:2017. The UK participation in i
2、ts preparation was entrusted to TechnicalCommittee IST/35, Health informatics.A list of organizations represented on this committee can beobtained on request to its secretary.This publication does not purport to include all the necessaryprovisions of a contract. Users are responsible for its correct
3、application. The British Standards Institution 2017. Published by BSI Standards Limited 2017ISBN 978 0 580 83466 0ICS 35.240.80Compliance with a British Standard cannot confer immunity fromlegal obligations.This British Standard was published under the authority of theStandards Policy and Strategy C
4、ommittee on 31 January 2017.Amendments/Corrigenda issued since publicationDate Text affectedEUROPEAN STANDARD NORME EUROPENNE EUROPISCHE NORM EN ISO 25237 January 2017 ICS 35.240.80 English Version Health informatics - Pseudonymization (ISO 25237:2017) Informatique de sant - Pseudonymisation (ISO 25
5、237:2017) Medizinische Informatik - Pseudonymisierung (ISO 25237:2017) This European Standard was approved by CEN on 14 December 2016. CEN members are bound to comply with the CEN/CENELEC Internal Regulations which stipulate the conditions for giving this European Standard the status of a national s
6、tandard without any alteration. Up-to-date lists and bibliographical references concerning such national standards may be obtained on application to the CEN-CENELEC Management Centre or to any CEN member. This European Standard exists in three official versions (English, French, German). A version i
7、n any other language made by translation under the responsibility of a CEN member into its own language and notified to the CEN-CENELEC Management Centre has the same status as the official versions. CEN members are the national standards bodies of Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech
8、Republic, Denmark, Estonia, Finland, Former Yugoslav Republic of Macedonia, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and United Kingd
9、om. EUROPEAN COMMITTEE FOR STANDARDIZATION COMIT EUROPEN DE NORMALISATION EUROPISCHES KOMITEE FR NORMUNG CEN-CENELEC Management Centre: Avenue Marnix 17, B-1000 Brussels 2017 CEN All rights of exploitation in any form and by any means reserved worldwide for CEN national Members. Ref. No. EN ISO 2523
10、7:2017 EBS EN ISO 25237:2017EN ISO 25237:2017 (E) Type de document : Norme europenne Sous-type de document : Stade du document : Publication / Adoption Langue du document : E Y:STD_MGTSTDDELPRODUCTIONStandards0025131664_e_stf.doc STD Version 2.5a European foreword This document (EN ISO 25237:2017) h
11、as been prepared by Technical Committee ISO/TC 215 “Health informatics” in collaboration with Technical Committee CEN/TC 251 “Health informatics” the secretariat of which is held by NEN. This European Standard shall be given the status of a national standard, either by publication of an identical te
12、xt or by endorsement, at the latest by July 2017, and conflicting national standards shall be withdrawn at the latest by July 2017. Attention is drawn to the possibility that some of the elements of this document may be the subject of patent rights. CEN and/or CENELEC shall not be held responsible f
13、or identifying any or all such patent rights. According to the CEN-CENELEC Internal Regulations, the national standards organizations of the following countries are bound to implement this European Standard: Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, Form
14、er Yugoslav Republic of Macedonia, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and the United Kingdom. Endorsement notice The text of IS
15、O 25237:2017 has been approved by CEN as EN ISO 25237:2017 without any modification. BS EN ISO 25237:2017ISO 25237:2017(E)Foreword vIntroduction vi1 Scope . 12 Normative references 13 Terms and definitions . 14 Abbreviated terms 65 Requirements for privacy protection of identities in healthcare 75.1
16、 Objectives of privacy protection 75.2 General . 75.3 De-identification as a process to reduce risk 85.3.1 General 85.3.2 Pseudonymization 85.3.3 Anonymization 95.3.4 Direct and indirect identifiers 95.4 Privacy protection of entities . 95.4.1 Personal data versus de-identified data 95.4.2 Concept o
17、f pseudonymization . 115.5 Real world pseudonymization 135.5.1 Rationale 135.5.2 Levels of assurance of privacy protection .145.6 Categories of data subject . 165.6.1 General. 165.6.2 Subject of care .165.6.3 Health professionals and organizations .165.6.4 Device data .165.7 Classification data . 17
18、5.7.1 Payload data 175.7.2 Observational data 175.7.3 Pseudonymized data .175.7.4 Anonymized data 175.8 Research data 175.8.1 General. 175.8.2 Generation of research data 185.8.3 Secondary use of personal health information .185.9 Identifying data . 185.9.1 General. 185.9.2 Healthcare identifiers .1
19、85.10 Data of victims of violence and publicly known persons 195.10.1 General. 195.10.2 Genetic information .195.10.3 Trusted service .195.10.4 Need for re-identification of pseudonymized data .195.10.5 Pseudonymization service characteristics .206 Protecting privacy through pseudonymization .206.1
20、Conceptual model of the problem areas 206.2 Direct and indirect identifiability of personal information .216.2.1 General. 216.2.2 Person identifying variables . 216.2.3 Aggregation variables .216.2.4 Outlier variables 226.2.5 Structured data variables 226.2.6 Non-structured data variables 23 ISO 201
21、7 All rights reserved iiiContents PageBS EN ISO 25237:2017ISO 25237:2017(E)6.2.7 Inference risk assessment 236.2.8 Privacy and security .247 Re-identification process 247.1 General 247.2 Part of normal procedures . 247.3 Exception. 247.4 Technical feasibility . 25Annex A (informative) Healthcare pse
22、udonymization scenarios 26Annex B (informative) Requirements for privacy risk analysis 39Annex C (informative) Pseudonymization process (methods and implementation) .49Annex D (informative) Specification of methods and implementation .55Annex E (informative) Policy framework for operation of pseudon
23、ymization services (methods and implementation) 56Annex F (informative) Genetic information .60Bibliography .61iv ISO 2017 All rights reservedBS EN ISO 25237:2017ISO 25237:2017(E)ForewordISO (the International Organization for Standardization) is a worldwide federation of national standards bodies (
24、ISO member bodies). The work of preparing International Standards is normally carried 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, go
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