Document Center List of Standards on Medical Microbiology Laboratory Medicine, See 11.100
ICS Code 07.100.10
Return to ICS Index.Up to Level 2:
The following documents are a part of this series:
ASTM:
- ASTM-D3870 - Standard Practice for Establishing Performance Characteristics for Colony Counting Methods in Microbiology (Withdrawn 2000)
- ASTM-D4198 - Standard Test Methods for Evaluating Absorbent Pads Used with Membrane Filters for Bacteriological Analysis and Growth
- ASTM-D5952 - Standard Guide for the Inspection of Water Systems for Legionella and the Investigation of Possible Outbreaks of Legionellosis (Legionnaires' Disease or Pontiac Fever) (Withdrawn 2024)
- ASTM-E1280 - Standard Guide for Performing the Mouse Lymphoma Assay for Mammalian Cell Mutagenicity (Withdrawn 2015)
- ASTM-E1285 - Standard Guide for Identification of Bacteriophage Lambda (λ) or Its DNA (Withdrawn 2014)
- ASTM-E1286 - Standard Guide for Identification of Herpes Simplex Virus or Its DNA (Withdrawn 2014)
- ASTM-E1326 - Standard Guide for Evaluating Non-culture Microbiological Tests
- ASTM-E1532 - Standard Practice for Detection of Mycoplasma Contamination of Cell Cultures by Use of Bisbenzamide DNA-Binding Fluorochrome (Withdrawn 2014)
- ASTM-E1533 - Standard Practice for Indirect Detection of Mycoplasma in Cell Culture by 4`-6-Diamidino-2-2 Phenylindole (DAPI) Staining (Withdrawn 2014)
- ASTM-E1535 - Standard Test Method for Performance Evaluation of Anaerobic Digestion Systems (Withdrawn 2011)
- ASTM-E1536 - Standard Practice for Detection of Mycoplasma Contamination of Bovine Serum by Large Volume Method (Withdrawn 2014)
- ASTM-E1847 - Standard Practice for Statistical Analysis of Toxicity Tests Conducted Under ASTM Guidelines (Withdrawn 2022)
- ASTM-E1881 - Standard Guide for Cell Culture Analysis with SIMS
- ASTM-E1968 - Standard Practice for Microcrystal Testing in Forensic Analysis for Cocaine
- ASTM-E2097 - Standard Guide for Determining the Impact of Extractables from Non-Metallic Materials on the Safety of Biotechnology Products (Withdrawn 2022)
- ASTM-E2125 - Standard Practice for Microcrystal Testing in Forensic Analysis for Phencyclidine and Its Analogues
- ASTM-E2525 - Standard Test Method for Evaluation of the Effect of Nanoparticulate Materials on the Formation of Mouse Granulocyte-Macrophage Colonies
- ASTM-E2526 - Standard Test Method for Evaluation of Cytotoxicity of Nanoparticulate Materials in Porcine Kidney Cells and Human Hepatocarcinoma Cells
- ASTM-F2148 - Standard Practice for Evaluation of Delayed Contact Hypersensitivity Using the Murine Local Lymph Node Assay (LLNA)
- ASTM-F2997 - Standard Practice for Quantification of Calcium Deposits in Osteogenic Culture of Progenitor Cells Using Fluorescent Image Analysis
- ASTM-F665 - Standard Classification for Vinyl Chloride Plastics Used in Biomedical Application
- ASTM-F813 - Standard Practice for Direct Contact Cell Culture Evaluation of Materials for Medical Devices
- ASTM-F895 - Standard Test Method for Agar Diffusion Cell Culture Screening for Cytotoxicity
BSI:
- BS-5213 - Medical Specimen Containers for Microbiology, Specification For
- BS-EN-1174-1 - Part 1: Requirements, Sterilization of Medical Devices, Estimations of the Population Of
- BS-EN-1174-2 - Part 2: Guidance, Sterilization of Medical Devices, Estimation of the Population of Micro
- BS-EN-1174-3 - Sterilization of medical devices. Estimation of the population of micro-organisms on product
- BS-EN-12322 - In vitro diagnostic medical devices. Culture media for microbiology. Performance criteria for culture media
- BS-EN-1659 - In vitro diagnostic systems. Culture media for microbiology. Terms and definitions
- BS-EN-ISO-11737-1 - Sterilization of health care products. Microbiological methods
- BS-EN-ISO-11737-2 - Sterilization of health care products. Microbiological methods
- BS-ISO-11737-3 - Sterilization of health care products. Microbiological methods
- PD-ISO-22456 - Sterilization of healthcare products. Microbiological methods. Guidance on conducting bioburden determinations and tests of sterility for biologics and tissue-based products
ISO:
- ISO-11737-1 - Sterilization of health care products - Microbiological methods - Part 1: Determination of a population of microorganisms on products
- ISO-11737-1-AM1 - - Amendment 1
- ISO-11737-2 - Sterilization of health care products - Microbiological methods - Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process
- ISO-11737-3 - Sterilization of health care products - Microbiological methods - Part 3: Bacterial endotoxin testing
- ISO-22456 - Sterilization of healthcare products - Microbiological methods. Guidance on conducting bioburden determinations and tests of sterility for biologics and tissue-based products
Other SDOs:
- AAMI/ISO-TIR22442-4 - Medical devices utilizing animal tissues and their derivatives - Part 4: Principles for elimination and/or inactivation of transmissible spongiform encephalopathy (TSE) agents and validation assays for those processes
- ANSI/AAMI/ISO11737-1 - Sterilization Of Medical Devices - Microbiological Methods - Part 1: Determination Of A Population Of Microorganisms On Products
- ANSI/AAMI/ISO11737-2 - Sterilization of medical devices - Microbiological methods - Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process
- ANSI/AAMI/ISO11737-3 - Sterilization Of Medical Devices - Microbiological Methods - Part 3: Guidance On Evaluation and Interpretation Of Bioburden Data
- DIN-EN-ISO-11737-1 - Sterilization of health care products - Microbiological methods - Part 1: Determination of a population of microorganisms on products (ISO 11737-1:2018)
- EN-ISO-11737-1 - Part 1: Determination of a Population of Microorganisms on Products, Sterilization Of
- EN-ISO-11737-2 - Part 2: Tests of Sterility Performed in the Definition, Validation & Maintenance of A
- EN-ISO-18153 - In Vitro Diagnostic Medical Devices, Measurement of Quantities in Biological Samples -
- JIS-Z-2801 - Antibacterial products -- Test for antibacterial activity and efficacy
- SS-EN-1174-1 - Sterilization of medical devices - Estimation of the population of micro-organisms on product - Part 1: Requirements
- SS-EN-12322 - In vitro diagnostic medical devices - Culture media for microbiology - Performance criteria for culture media
- SS-EN-12322-AM1 - In vitro diagnostic medical devices - Culture media for microbiology - Performance criteria for culture media
- SS-EN-14254 - In vitro diagnostic medical devices - Single-use receptacles for the collection of specimens, other than blood, from humans
- SS-EN-1659 - In vitro diagnostic systems - Culture media for microbiology - Terms and definitions
- SS-EN-ISO-11737-1 - Sterilization of health care products - Microbiological methods - Part 1: Determination of a population of microorganisms on products (ISO 11737-1:2018)
- SS-EN-ISO-11737-1-AM1 - Sterilization of health care products - Microbiological methods - Part 1: Determination of a population of microorganisms on products - Amendment 1 (ISO 11737-1:2018/Amd 1:2021)
- SS-EN-ISO-11737-2 - Sterilization of health care products - Microbiological methods - Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process (ISO 11737-2:2019)
- SS-EN-ISO-15195 - Laboratory medicine - Requirements for the competence of calibration laboratories using reference measurement procedures (ISO 15195:2018)
- SS-EN-ISO-17511 - In vitro diagnostic medical devices - Requirements for establishing metrological traceability of values assigned to calibrators, trueness control materials and human samples (ISO 17511:2020)
- SS-EN-ISO-18153 - In vitro diagnostic medical devices - Measurement of quantities in biological samples - Metrological traceability of values for catalytic concentration of enzymes assigned to calibrators and control materials (ISO 18153:2003)
- SS-EN-ISO-6717 - In vitro diagnostic medical devices - Single-use containers for the collection of specimens from humans other than blood (ISO 6717:2021)