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ECCMA is the project leader for ISO 22745 (Open technical dictionaries and their application to master data). It also leads projects for developing sections of ISO 8000 (Data quality) and ISO 25500 (Supply chain interoperability and integration). These standards ensure data quality, and facilitate the exchange of material and service master data.
The process of using concept identifiers from an external open technical dictionary is a form of semantic encoding compliant with the requirements of ISO 8000-110:2008, the international standard for the exchange of quality master data. The eOTD concept identifiers are in the public domain.
An example SDS, including guidance for handling a hazardous substance and information on its composition and properties. A safety data sheet (SDS), [1] material safety data sheet (MSDS), or product safety data sheet (PSDS) is a document that lists information relating to occupational safety and health for the use of various substances and products.
ISO 22745 Industrial automation systems and integration - Open technical dictionaries and their application to master data ISO 22745-2:2010 Part 2: Vocabulary; ISO/IEC TR 22767:2005 Information technology – Telecommunications and information exchange between systems – Using CSTA for SIP phone user agents (uaCSTA)
Global Medical Device Nomenclature (GMDN) is a system of internationally agreed generic descriptors used to identify all medical device products. This nomenclature is a naming system for products which include those used for the diagnosis, prevention, monitoring, treatment or alleviation of disease or injury in humans.
Medical equipment management (sometimes referred to as clinical engineering, clinical engineering management, clinical technology management, healthcare technology management, biomedical maintenance, biomedical equipment management, and biomedical engineering) is a term for the professionals who manage operations, analyze and improve utilization and safety, and support servicing healthcare ...
These safety phrases were used internationally and not just in Europe, and there is an ongoing effort towards complete international harmonization. This harmonization would be carried out by the United Nations 's Globally Harmonized System of Classification and Labelling of Chemicals , that replaced Directive 67/548/EEC under CLP Regulation .
The United States Food and Drug Administration publishes a Data Standards Catalog that lists the data standards and terminologies that FDA supports for use in regulatory submissions to better enable the evaluation of safety, effectiveness, and quality of FDA-regulated products.