BSI PD ISO/TS 17975:2022
$167.15
Health informatics. Principles and data requirements for consent in the collection, use or disclosure of personal health information
| Published By | Publication Date | Number of Pages |
| BSI | 2022 | 44 |
PDF Catalog
| PDF Pages | PDF Title |
|---|---|
| 2 | National foreword |
| 6 | Foreword |
| 7 | Introduction |
| 11 | 1 Scope |
| 12 | 2 Normative references 3 Terms and definitions |
| 16 | 4 Abbreviated terms 5 Consent requirements 5.1 General |
| 17 | 5.2 Informational consent 5.3 Consent to treatment versus informational consent 5.4 How consent relates to privacy, duty of confidence and to authorization |
| 18 | 5.5 Relationship of consent to OECD guidelines 5.6 Relationship of consent to legislation 5.7 Expectations and rights of the individual |
| 19 | 5.8 Consent directives 5.9 Consent is related strongly to purpose of use |
| 20 | 5.10 Consent to collect and use versus consent to disclose 5.11 Consent is applicable to specified data |
| 21 | 5.12 Consent related to disclosure 5.13 Exceptional access |
| 22 | 5.14 Challenges associated with obtaining consent 6 Consent frameworks 6.1 Giving consent |
| 24 | 6.2 Types of consent sta |
| 25 | 6.3 Detailed requirements 6.3.1 Express or expressed (informed) consent |
| 26 | 6.3.2 Implied (informed) consent |
| 28 | 6.3.3 No consent sought |
| 29 | 6.3.4 Assumed consent (deemed consent) 7 Mechanisms and process: denial, opt-in and opt-out, and override 7.1 Express or expressed (and informed) denial |
| 31 | 7.2 Opt-in and opt-out 7.2.1 General 7.2.2 Opt-in 7.2.3 Opt-out 7.3 Override 8 Minimum data requirements |
| 33 | Annex A (informative) Consent framework diagrams |
| 39 | Annex B (informative) Jurisdictional implementation examples |
| 43 | Bibliography |
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