{"id":430883,"date":"2024-10-20T07:25:13","date_gmt":"2024-10-20T07:25:13","guid":{"rendered":"https:\/\/pdfstandards.shop\/product\/uncategorized\/bs-iso-204042023\/"},"modified":"2024-10-26T14:06:04","modified_gmt":"2024-10-26T14:06:04","slug":"bs-iso-204042023","status":"publish","type":"product","link":"https:\/\/pdfstandards.shop\/product\/publishers\/bsi\/bs-iso-204042023\/","title":{"rendered":"BS ISO 20404:2023"},"content":{"rendered":"
PDF Pages<\/th>\n | PDF Title<\/th>\n<\/tr>\n | ||||||
---|---|---|---|---|---|---|---|
2<\/td>\n | National foreword <\/td>\n<\/tr>\n | ||||||
6<\/td>\n | Foreword <\/td>\n<\/tr>\n | ||||||
7<\/td>\n | Introduction <\/td>\n<\/tr>\n | ||||||
9<\/td>\n | 1 Scope 2 Normative references 3 Terms and definitions <\/td>\n<\/tr>\n | ||||||
11<\/td>\n | 4 General strategy for packaging design 4.1 General <\/td>\n<\/tr>\n | ||||||
12<\/td>\n | 4.2 Configuration of cells for therapeutic use 4.2.1 General 4.2.2 Suspension of cells 4.2.3 Tissue <\/td>\n<\/tr>\n | ||||||
13<\/td>\n | 4.3 Process of containing cells for therapeutic use in packaging 4.4 Disturbances in storage and transportation including contamination 4.5 Impact on external environment when cells for therapeutic use leak from packaging 4.6 Interaction between cells for therapeutic use and packaging 4.7 Usability of packaging in clinical facilities 4.8 Environmental impact 5 Design for packaging 5.1 General 5.2 Enclosing process 5.2.1 Explanation of the enclosing process <\/td>\n<\/tr>\n | ||||||
14<\/td>\n | 5.2.2 Packaging for the enclosing process 5.3 Processes from enclosing to usage 5.3.1 Disturbances that affect cells for therapeutic use <\/td>\n<\/tr>\n | ||||||
15<\/td>\n | 5.3.2 Leakage 5.3.3 Interactions between cells for therapeutic use and packaging <\/td>\n<\/tr>\n | ||||||
17<\/td>\n | 5.4 Usage <\/td>\n<\/tr>\n | ||||||
18<\/td>\n | 6 Implementing packaging design 6.1 General 6.2 Shape <\/td>\n<\/tr>\n | ||||||
19<\/td>\n | 6.3 Layers 6.4 Ports 6.5 Packaging materials 6.6 Communication between packaging supplier and packaging user <\/td>\n<\/tr>\n | ||||||
20<\/td>\n | 7 Quality management 8 Examples of test methods 8.1 General 8.2 Test methods related to disturbance 8.3 Test methods related to leakage 8.4 Test methods related to interaction between cells for therapeutic use and packaging <\/td>\n<\/tr>\n | ||||||
21<\/td>\n | 8.5 Other test methods <\/td>\n<\/tr>\n | ||||||
23<\/td>\n | Annex A (informative) Illustrated examples of packaging, packages and shipping containers <\/td>\n<\/tr>\n | ||||||
26<\/td>\n | Bibliography <\/td>\n<\/tr>\n<\/table>\n","protected":false},"excerpt":{"rendered":" Biotechnology. Bioprocessing. General requirements for the design of packaging to contain cells for therapeutic use<\/b><\/p>\n |