{"id":279663,"date":"2024-10-19T18:52:52","date_gmt":"2024-10-19T18:52:52","guid":{"rendered":"https:\/\/pdfstandards.shop\/product\/uncategorized\/bs-en-iso-11138-72019\/"},"modified":"2024-10-25T15:26:58","modified_gmt":"2024-10-25T15:26:58","slug":"bs-en-iso-11138-72019","status":"publish","type":"product","link":"https:\/\/pdfstandards.shop\/product\/publishers\/bsi\/bs-en-iso-11138-72019\/","title":{"rendered":"BS EN ISO 11138-7:2019"},"content":{"rendered":"
This document provides guidance for the selection, use and interpretation of results from application of biological indicators when used in the development, validation and routine monitoring of sterilization processes.<\/p>\n
It does not consider those processes that rely solely on physical removal of microorganisms, e.g. filtration.<\/p>\n
It is not applicable to combination processes using, for example, washer-disinfectors or flushing and steaming of pipelines.<\/p>\n
It does not specify requirements for the selection and use of biological indicators intended to monitor vaporised hydrogen peroxide processes for isolator and room biodecontamination processes at atmospheric pressure.<\/p>\n
It is not applicable to liquid immersion sterilization processes.<\/p>\n
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 | ||||||
7<\/td>\n | Foreword <\/td>\n<\/tr>\n | ||||||
8<\/td>\n | Introduction <\/td>\n<\/tr>\n | ||||||
9<\/td>\n | 1 Scope 2 Normative references 3 Terms and definitions <\/td>\n<\/tr>\n | ||||||
12<\/td>\n | 4 General <\/td>\n<\/tr>\n | ||||||
14<\/td>\n | 5 Characteristics of biological indicators 5.1 General <\/td>\n<\/tr>\n | ||||||
15<\/td>\n | 5.2 Test organism suspension for direct inoculation of products 5.3 Inoculated carriers <\/td>\n<\/tr>\n | ||||||
16<\/td>\n | 5.4 Self-contained biological indicators 6 Selection of supplier 6.1 General <\/td>\n<\/tr>\n | ||||||
17<\/td>\n | 6.2 Documentation 6.2.1 General <\/td>\n<\/tr>\n | ||||||
18<\/td>\n | 6.2.2 Manufacturer audit <\/td>\n<\/tr>\n | ||||||
19<\/td>\n | 7 Biological indicators in process development 7.1 General 7.2 Overkill approach <\/td>\n<\/tr>\n | ||||||
20<\/td>\n | 7.3 Combined biological indicator and bioburden method <\/td>\n<\/tr>\n | ||||||
21<\/td>\n | 7.4 Bioburden method 8 Biological indicators in sterilization validation 8.1 General <\/td>\n<\/tr>\n | ||||||
22<\/td>\n | 8.2 Placement and handling of biological indicators 8.3 Sterilizer qualification 8.4 Performance qualification <\/td>\n<\/tr>\n | ||||||
23<\/td>\n | 8.5 Review and approval of validation 8.6 Requalification 9 Biological indicators in routine monitoring 9.1 General <\/td>\n<\/tr>\n | ||||||
24<\/td>\n | 9.2 Placement and handling of biological indicators 9.3 Process challenge device <\/td>\n<\/tr>\n | ||||||
25<\/td>\n | 10 Interpretation and acceptance criteria 10.1 General 10.2 Interpretation of results 11 Application of biological indicator standards 11.1 General assessment of biological indicator performance by the user <\/td>\n<\/tr>\n | ||||||
26<\/td>\n | 11.2 Nominal population of test organism <\/td>\n<\/tr>\n | ||||||
27<\/td>\n | 11.3 Resistance determination 11.3.1 General 11.3.2 Survivor curve method 11.3.3 Fraction-negative method <\/td>\n<\/tr>\n | ||||||
28<\/td>\n | 11.3.4 Survival-kill response characteristics 11.4 z value determination 11.4.1 General 11.4.2 Graphically plotting the z value <\/td>\n<\/tr>\n | ||||||
29<\/td>\n | 11.4.3 Mathematically calculating the z value <\/td>\n<\/tr>\n | ||||||
30<\/td>\n | 11.4.4 Correlation coefficient, r, for the z value 11.5 F(T, z) equivalent sterilization value determination 11.6 Establishing spore-log-reduction <\/td>\n<\/tr>\n | ||||||
31<\/td>\n | 11.7 Sterility assurance level calculation 11.8 Test equipment <\/td>\n<\/tr>\n | ||||||
32<\/td>\n | 12 Culture conditions 12.1 General 12.2 Incubation temperature 12.3 Incubation period <\/td>\n<\/tr>\n | ||||||
33<\/td>\n | 12.4 Choice of growth medium 13 Third-party considerations 13.1 General <\/td>\n<\/tr>\n | ||||||
34<\/td>\n | 13.2 Minimum requirements from ISO 11138-1 for replicates and total number of biological indicators 13.3 Test equipment 14 Personnel training <\/td>\n<\/tr>\n | ||||||
35<\/td>\n | 15 Storage and handling 16 Disposal of biological indicators <\/td>\n<\/tr>\n | ||||||
36<\/td>\n | Annex A (informative) Microbiological inactivation kinetics and enumeration techniques <\/td>\n<\/tr>\n | ||||||
41<\/td>\n | Annex B (informative) Process challenge devices <\/td>\n<\/tr>\n | ||||||
42<\/td>\n | Annex C (informative) Formulae for D value determination by fraction-negative method <\/td>\n<\/tr>\n | ||||||
58<\/td>\n | Annex D (informative) Examples of documentation for biological indicators prepared by the user <\/td>\n<\/tr>\n | ||||||
62<\/td>\n | Annex E (informative) Calculation of z value <\/td>\n<\/tr>\n | ||||||
65<\/td>\n | Annex F (informative) D value determination by survivor curve method <\/td>\n<\/tr>\n | ||||||
69<\/td>\n | Annex G (informative) Survival-kill response characteristics <\/td>\n<\/tr>\n | ||||||
71<\/td>\n | Bibliography <\/td>\n<\/tr>\n<\/table>\n","protected":false},"excerpt":{"rendered":" Sterilization of health care products. Biological indicators – Guidance for the selection, use and interpretation of results<\/b><\/p>\n |