{"id":418753,"date":"2024-10-20T06:22:36","date_gmt":"2024-10-20T06:22:36","guid":{"rendered":"https:\/\/pdfstandards.shop\/product\/uncategorized\/bsi-pd-iso-ts-179752022-tc\/"},"modified":"2024-10-26T11:54:11","modified_gmt":"2024-10-26T11:54:11","slug":"bsi-pd-iso-ts-179752022-tc","status":"publish","type":"product","link":"https:\/\/pdfstandards.shop\/product\/publishers\/bsi\/bsi-pd-iso-ts-179752022-tc\/","title":{"rendered":"BSI PD ISO\/TS 17975:2022 – TC"},"content":{"rendered":"
PDF Pages<\/th>\n | PDF Title<\/th>\n<\/tr>\n | ||||||
---|---|---|---|---|---|---|---|
1<\/td>\n | 30466325 <\/td>\n<\/tr>\n | ||||||
59<\/td>\n | A-30442718 <\/td>\n<\/tr>\n | ||||||
60<\/td>\n | National foreword <\/td>\n<\/tr>\n | ||||||
64<\/td>\n | Foreword <\/td>\n<\/tr>\n | ||||||
65<\/td>\n | Introduction <\/td>\n<\/tr>\n | ||||||
69<\/td>\n | 1 Scope <\/td>\n<\/tr>\n | ||||||
70<\/td>\n | 2 Normative references 3 Terms and definitions <\/td>\n<\/tr>\n | ||||||
74<\/td>\n | 4 Abbreviated terms 5 Consent requirements 5.1 General <\/td>\n<\/tr>\n | ||||||
75<\/td>\n | 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 <\/td>\n<\/tr>\n | ||||||
76<\/td>\n | 5.5 Relationship of consent to OECD guidelines 5.6 Relationship of consent to legislation 5.7 Expectations and rights of the individual <\/td>\n<\/tr>\n | ||||||
77<\/td>\n | 5.8 Consent directives 5.9 Consent is related strongly to purpose of use <\/td>\n<\/tr>\n | ||||||
78<\/td>\n | 5.10 Consent to collect and use versus consent to disclose 5.11 Consent is applicable to specified data <\/td>\n<\/tr>\n | ||||||
79<\/td>\n | 5.12 Consent related to disclosure 5.13 Exceptional access <\/td>\n<\/tr>\n | ||||||
80<\/td>\n | 5.14 Challenges associated with obtaining consent 6 Consent frameworks 6.1 Giving consent <\/td>\n<\/tr>\n | ||||||
82<\/td>\n | 6.2 Types of consent sta <\/td>\n<\/tr>\n | ||||||
83<\/td>\n | 6.3 Detailed requirements 6.3.1 Express or expressed (informed) consent <\/td>\n<\/tr>\n | ||||||
84<\/td>\n | 6.3.2 Implied (informed) consent <\/td>\n<\/tr>\n | ||||||
86<\/td>\n | 6.3.3 No consent sought <\/td>\n<\/tr>\n | ||||||
87<\/td>\n | 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 <\/td>\n<\/tr>\n | ||||||
89<\/td>\n | 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 <\/td>\n<\/tr>\n | ||||||
91<\/td>\n | Annex A (informative) Consent framework diagrams <\/td>\n<\/tr>\n | ||||||
97<\/td>\n | Annex B (informative) Jurisdictional implementation examples <\/td>\n<\/tr>\n | ||||||
101<\/td>\n | Bibliography <\/td>\n<\/tr>\n<\/table>\n","protected":false},"excerpt":{"rendered":" Tracked Changes. Health informatics. Principles and data requirements for consent in the collection, use or disclosure of personal health information<\/b><\/p>\n |