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The consortium for Standardization in Lab Automation (SiLA) is a not-for-profit membership organization formed by software suppliers, system integrators and pharma/biotech companies. It develops and introduces new device and data interface standards allowing rapid integration of lab automation hardware and data management systems. Highly ...
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Name of the laboratory equipment item image An image illustrating the item alt Alternative text for the image (see Wikipedia:Alternative text for images) caption Caption for the image acronym Acronym or abbreviation for the item other_names Any other names used for this item uses
ISO/IEC 17025 General requirements for the competence of testing and calibration laboratories is the main standard used by testing and calibration laboratories. In most countries, ISO/IEC 17025 is the standard for which most labs must hold accreditation in order to be deemed technically competent.
This standard was subsequently revised in 1978 (IEEE-488.1) and 1990 (IEEE-488.2). The IEEE 488.2 specification includes the Standard Commands for Programmable Instrumentation (SCPI), which define specific commands that each instrument class must obey. SCPI ensures compatibility and configurability among these instruments.
ISO 15189 Medical laboratories — Requirements for quality and competence is an international standard that specifies the quality management system requirements particular to medical laboratories. The standard was developed by the International Organisation for Standardization 's Technical Committee 212 (ISO/TC 212).
IEC 60477 Laboratory d.c. resistors; IEC 60479 Effects of current on human beings and livestock; IEC 60480 Guidelines for the checking and treatment of sulfur hexafluoride (SF6) taken from electrical equipment and specification for its re-use; IEC 60481 Coupling devices for power line carrier systems
Laboratory Data Model (LAB) The Lab standard is used for the exchange of laboratory data between labs and CROs; Case Report Tabulation Data Definition Specification (CRT-DDS) Also referred to as "define.xml", a machine readable version of the regulatory submission "define.pdf". Clinical Data Acquisition Standards Harmonization (CDASH) [6]
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