{"id":426105,"date":"2024-10-20T07:00:16","date_gmt":"2024-10-20T07:00:16","guid":{"rendered":"https:\/\/pdfstandards.shop\/product\/uncategorized\/bsi-pd-cen-iso-ts-172512023\/"},"modified":"2024-10-26T13:14:10","modified_gmt":"2024-10-26T13:14:10","slug":"bsi-pd-cen-iso-ts-172512023","status":"publish","type":"product","link":"https:\/\/pdfstandards.shop\/product\/publishers\/bsi\/bsi-pd-cen-iso-ts-172512023\/","title":{"rendered":"BSI PD CEN ISO\/TS 17251:2023"},"content":{"rendered":"
PDF Pages<\/th>\n | PDF Title<\/th>\n<\/tr>\n | ||||||
---|---|---|---|---|---|---|---|
2<\/td>\n | undefined <\/td>\n<\/tr>\n | ||||||
4<\/td>\n | European foreword Endorsement notice <\/td>\n<\/tr>\n | ||||||
6<\/td>\n | Foreword <\/td>\n<\/tr>\n | ||||||
8<\/td>\n | Introduction <\/td>\n<\/tr>\n | ||||||
9<\/td>\n | 1 Scope 2 Normative references <\/td>\n<\/tr>\n | ||||||
10<\/td>\n | 3 Terms and definitions <\/td>\n<\/tr>\n | ||||||
12<\/td>\n | 4 Relationship to other ISO deliverables <\/td>\n<\/tr>\n | ||||||
13<\/td>\n | 5 Conformance 6 Business requirements for structured dose instructions 6.1 General 6.2 Use cases 6.3 Elements of a dose instruction <\/td>\n<\/tr>\n | ||||||
15<\/td>\n | 6.4 Information requirements 6.4.1 General 6.4.2 Terminologies and Code Systems 6.4.3 Information model <\/td>\n<\/tr>\n | ||||||
16<\/td>\n | 6.4.4 Text representation 6.4.5 Administration amount <\/td>\n<\/tr>\n | ||||||
17<\/td>\n | 6.4.6 Route\/site of administration 6.4.7 Timing of dose event(s) <\/td>\n<\/tr>\n | ||||||
19<\/td>\n | 6.4.8 Conditional administration 6.4.9 Subject of care-specific information <\/td>\n<\/tr>\n | ||||||
20<\/td>\n | 6.4.10 Ancillary information <\/td>\n<\/tr>\n | ||||||
22<\/td>\n | Bibliography <\/td>\n<\/tr>\n<\/table>\n","protected":false},"excerpt":{"rendered":" Health informatics. Business requirements for a syntax to exchange structured dose information for medicinal products<\/b><\/p>\n |