Recognized Consensus Standards: Medical Devices
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1 to 10 of 115 Results
Specialty Task Group Area: InVitro Diagnostics |
Results per Page |
Date of
Entry |
Specialty Task
Group Area |
Recognition
Number |
Extent of
Recognition |
Standards
Developing Organization |
Standard Designation Number and Date |
Standard Title (click for recognition information) |
05/29/2024 | InVitro Diagnostics | 7-321 | Partial | CLSI | MM24 1st Edition | Molecular Methods for Genotyping and Strain Typing of Infectious Organisms |
12/18/2023 | InVitro Diagnostics | 7-320 | Partial | CLSI | H62 1st Edition | Validation of Assays Performed by Flow Cytometry |
12/18/2023 | InVitro Diagnostics | 7-319 | Complete | CLSI | M23 6th Edition | Development of In Vitro Susceptibility Test Methods, Breakpoints, and Quality Control Parameters |
12/18/2023 | InVitro Diagnostics | 7-318 | Complete | CLSI | EP25 2nd Edition | Evaluation of Stability of In Vitro Medical Laboratory Test Reagents |
05/29/2023 | InVitro Diagnostics | 7-317 | Partial | CLSI | M100, 33rd Edition | Performance Standards for Antimicrobial Susceptibility Testing |
05/29/2023 | InVitro Diagnostics | 7-316 | Complete | CLSI | NBS01 7th Edition | Dried Blood Spot Specimen Collection for Newborn Screening |
05/29/2023 | InVitro Diagnostics | 7-315 | Complete | CLSI | EP12 3rd Edition | Evaluation of Qualitative, Binary Output Examination Performance |
12/19/2022 | InVitro Diagnostics | 7-314 | Partial | CLSI | M27M44S, 3rd Edition | Performance Standards for Antifungal Susceptibility Testing of Yeasts |
12/19/2022 | InVitro Diagnostics | 7-313 | Complete | CLSI | EP27 2nd Edition | Constructing and Interpreting an Error Grid for Quantitative Measurement Procedures |
05/30/2022 | InVitro Diagnostics | 7-312 | Complete | CLSI | M39 5th Edition | Analysis and Presentation of Cumulative Antimicrobial Susceptibility Test Data |
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