GB/T 43279.1-2023
分子体外诊断检验 静脉全血检验前过程的规范 第1部分:分离细胞RNA
Molecular in vitro diagnostic examinations—Specifications for pre-examination processes for venous whole blood—Part 1: Isolated cellular RNA
- 实施日期
- 2024-06-01
- ICS 分类
- 11.100.10
组合使用关键词、标准类型、状态与 ICS 分类,快速定位所需国家标准。
找到 167 条
GB/T 43279.1-2023
Molecular in vitro diagnostic examinations—Specifications for pre-examination processes for venous whole blood—Part 1: Isolated cellular RNA
GB 19082-2023
Disposable protective clothing for medical use
GB 19083-2023
Protective face mask for medical use
GB/Z 16886.22-2022
Biological evaluation of medical devices—Part 22:Guidance on nanomaterials
GB/T 16886.19-2022
Biological evaluation of medical devices—Part 19: Physico-chemical, morphological and topographical characterization of materials
GB/T 16886.18-2022
Biological evaluation of medical devices—Part 18: Chemical characterization of medical device materials within a risk management process
GB/T 16886.15-2022
Biological evaluation of medical devices—Part 15: Identification and quantification of degradation products from metals and alloys
GB/T 16886.9-2022
Biological evaluation of medical devices—Part 9:Framework for identification and quantification of potential degradation products
GB/T 42080.2-2022
Molecular in vitro diagnostic examinations—Specifications for pre-examination processes for frozen tissue—Part2:Isolated proteins
GB/T 42080.1-2022
Molecular in vitro diagnostic examinations—Specifications for pre-examination processes for frozen tissue—Part 1: Isolated RNA
GB/T 42216.2-2022
Molecular in vitro diagnostic examinations—Specifications for pre-examination processes for formalin-fixed and paraffin-embedded(FFPE) tissue—Part 2:Isolated proteins
GB/T 42216.3-2022
Molecular in vitro diagnostic examinations—Specifications for pre-examination processes for formalin-fixed and paraffin-embedded (FFPE) tissue—Part 3:Isolated DNA
GB/T 42216.1-2022
Molecular in vitro diagnostic examinations—Specifications for pre-examination processes for formalin-fixed and paraffin-embedded (FFPE) tissue—Part 1:Isolated RNA
GB/T 42218-2022
Clinical laboratory medicine—In vitro diagnostic medical devices—Validation of user quality control procedures by the manufacturer
GB/T 21919-2022
Laboratory medicine—Requirements for the competence of calibration laboratories using reference measurement procedures
GB/T 42060-2022
Medical laboratories—Requirements for collection, transport, receipt, and handling of samples
GB 41918-2022
Biological safety cabinets
GB/T 16886.1-2022
Biological evaluation of medical devices—Part 1: Evaluation and testing within a risk management process
GB/T 16886.6-2022
Biological evaluation of medical devices—Part 6:Tests for local effects after implantation
GB/T 40966-2021
Quality assessment requirements for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antigen detection kit