发布时间：2024-05-27 17:49:26 - 更新时间：2024年06月29日 15:22
点击量：0
有样品要送检？试试一键送检，5分钟极速响应
在线提交检测需求
对接客服咨询检测
Sampling procedures used for acceptance testing of in vitro diagnostic medical devices - Statistical aspects.
IN VITRO DIAGNOSTIC MEDICAL DEVICES. CULTURE MEDIA FOR MICROBIOLOGY. PERFORMANCE CRITERIA FOR CULTURE MEDIA.
In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Presentation of reference measurement procedures
This European Standard specifies requirements for the drafting of a reference measurement procedure. NOTE It is intended that an experienced
In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Presentation of reference measurement procedures
This European Standard specifies requirements and formats for the description of reference materials. It is applicable to reference materials
In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Description of reference materials
In vitro diagnostic medical devices. Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology
This standard specifies requirements and test methods for single-use evacuated and non-evacuated receptacles, intended by their manufacturers
In vitro diagnostic medical devices - Single-use receptacles for the collection of specimens, other than blood, from humans
In vitro diagnostic medical devices — Information supplied by the manufacturer(labelling) — Part 4: In vitro diagnostic reagents for self-testing
CORRIGENDUM to the European Parliament and of the Council on in Vitro Diagnostic Medical Devices
In vitro diagnostic medical devices — Information supplied by the manufacturer(labelling) — Part 2: In vitro diagnostic reagents for professional use
In vitro diagnostic medical devices — Information supplied by the manufacturer(labelling) — Part 5: In vitro diagnostic instruments for self-testing
이 규격은 체외 진단 의료 기기의 제조자가 사용자에게 권장하는 정도 관리 절차의 타당성 확
Clinical laboratory medicine-In vitro diagnostic medical devices-Validation of user quality control procedures by the manufacturer
This International Standard describes a process for manufacturers of in vitro diagnostic medical devices to validate quality control procedures
Clinical laboratory medicine - In vitro diagnostic medical devices - Validation of user quality control procedures by the manufacturer
This International Standard describes a process for manufacturers of in vitro diagnostic medical devices to validate quality control procedures
Clinical laboratory medicine - In vitro diagnostic medical devices - Validation of user quality control procedures by the manufacturer
Clinical laboratory medicine — In vitro diagnostic medical devices — Validation of user quality control procedures by the manufacturer
Sampling procedures used for acceptance testing of in vitro diagnostic medical devices - Statistical aspects.
IN VITRO DIAGNOSTIC MEDICAL DEVICES. CULTURE MEDIA FOR MICROBIOLOGY. PERFORMANCE CRITERIA FOR CULTURE MEDIA.
In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Presentation of reference measurement procedures
This European Standard specifies requirements for the drafting of a reference measurement procedure. NOTE It is intended that an experienced
In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Presentation of reference measurement procedures
This European Standard specifies requirements and formats for the description of reference materials. It is applicable to reference materials
In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Description of reference materials
In vitro diagnostic medical devices. Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology
This standard specifies requirements and test methods for single-use evacuated and non-evacuated receptacles, intended by their manufacturers
In vitro diagnostic medical devices - Single-use receptacles for the collection of specimens, other than blood, from humans
In vitro diagnostic medical devices — Information supplied by the manufacturer(labelling) — Part 4: In vitro diagnostic reagents for self-testing
CORRIGENDUM to the European Parliament and of the Council on in Vitro Diagnostic Medical Devices
In vitro diagnostic medical devices — Information supplied by the manufacturer(labelling) — Part 2: In vitro diagnostic reagents for professional use
In vitro diagnostic medical devices — Information supplied by the manufacturer(labelling) — Part 5: In vitro diagnostic instruments for self-testing
이 규격은 체외 진단 의료 기기의 제조자가 사용자에게 권장하는 정도 관리 절차의 타당성 확
Clinical laboratory medicine-In vitro diagnostic medical devices-Validation of user quality control procedures by the manufacturer
This International Standard describes a process for manufacturers of in vitro diagnostic medical devices to validate quality control procedures
Clinical laboratory medicine - In vitro diagnostic medical devices - Validation of user quality control procedures by the manufacturer
This International Standard describes a process for manufacturers of in vitro diagnostic medical devices to validate quality control procedures
Clinical laboratory medicine - In vitro diagnostic medical devices - Validation of user quality control procedures by the manufacturer
Clinical laboratory medicine — In vitro diagnostic medical devices — Validation of user quality control procedures by the manufacturer
首页
点击咨询
