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Standard Guide for Electronic Authentication of Health Care Information (Withdrawn 2017)
Automaticky preložený názov:
Štandardné Sprievodca pre elektronické overovanie zdravotníckych informácií starostlivosti
NORMA vydaná dňa 1.3.2013
Označenie normy: ASTM E1762-95(2013)
Poznámka: NEPLATNÁ
Dátum vydania normy: 1.3.2013
Kód tovaru: NS-42943
Počet strán: 17
Približná hmotnosť: 51 g (0.11 libier)
Krajina: Americká technická norma
Kategória: Technické normy ASTM
Keywords:
accountability, authentication, authorization, biometric authentication, certificate, cryptography, data integrity, digital signature, electronic signature, non-repudiation, responsibility, timestamp, trusted third party, user identification, ICS Number Code 35.240.80 (IT applications in health care technology)
Significance and Use | ||||||||||||||||||
4.1 This guide serves three purposes: 4.1.1 To serve as a guide for developers of computer software providing, or interacting with, electronic signature processes, 4.1.2 To serve as a guide to healthcare providers who are implementing electronic signature mechanisms, and 4.1.3 To be a consensus standard on the design, implementation, and use of electronic signatures. |
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1. Scope | ||||||||||||||||||
1.1 This guide covers: 1.1.1 Defining a document structure for use by electronic signature mechanisms (Section 4), 1.1.2 Describing the characteristics of an electronic signature process (Section 5), 1.1.3 Defining minimum requirements for different electronic signature mechanisms (Section 5), 1.1.4 Defining signature attributes for use with electronic signature mechanisms (Section 6), 1.1.5 Describing acceptable electronic signature mechanisms and technologies (Section 1.1.6 Defining minimum requirements for user identification, access control, and other security requirements for electronic signatures (Section 9), and 1.1.7 Outlining technical details for all electronic signature mechanisms in sufficient detail to allow interoperability between systems supporting the same signature mechanism (Section 8 and Appendix X1-Appendix X4). 1.2 This guide is intended to be complementary to standards under development in other organizations. The determination of which documents require signatures is out of scope, since it is a matter addressed by law, regulation, accreditation standards, and an organization's policy. 1.3 Organizations shall develop policies and procedures that define the content of the medical record, what is a documented event, and what time constitutes event time. Organizations should review applicable statutes and regulations, accreditation standards, and professional practice guidelines in developing these policies and procedures. |
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2. Referenced Documents | ||||||||||||||||||
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