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  2. General MIDI - Wikipedia

    en.wikipedia.org/wiki/General_MIDI

    General MIDI (also known as GM or GM 1) is a standardized specification for electronic musical instruments that respond to MIDI messages. GM was developed by the American MIDI Manufacturers Association (MMA) and the Japan MIDI Standards Committee (JMSC) and first published in 1991. The official specification is available in English from the MMA ...

  3. Global Medical Device Nomenclature - Wikipedia

    en.wikipedia.org/wiki/Global_Medical_Device...

    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.

  4. List of abbreviations used in medical prescriptions - Wikipedia

    en.wikipedia.org/wiki/List_of_abbreviations_used...

    This is a list of abbreviations used in medical prescriptions, including hospital orders (the patient-directed part of which is referred to as sig codes).This list does not include abbreviations for pharmaceuticals or drug name suffixes such as CD, CR, ER, XT (See Time release technology § List of abbreviations for those).

  5. Genetically modified food - Wikipedia

    en.wikipedia.org/wiki/Genetically_modified_food

    This is an accepted version of this page This is the latest accepted revision, reviewed on 15 August 2024. Foods produced from organisms that have had changes introduced into their DNA Part of a series on Genetic engineering Genetically modified organisms Bacteria Viruses Animals Mammals Fish Insects Plants Maize/corn Rice Soybean Potato History and regulation History Regulation Substantial ...

  6. Cartagena Protocol on Biosafety - Wikipedia

    en.wikipedia.org/wiki/Cartagena_Protocol_on_Bio...

    In accordance with the precautionary approach, contained in Principle 15 of the Rio Declaration on Environment and Development, the objective of the Protocol is to contribute to ensuring an adequate level of protection in the field of the safe transfer, handling and use of 'living modified organisms resulting from modern biotechnology' that may ...

  7. Production part approval process - Wikipedia

    en.wikipedia.org/wiki/Production_part_approval...

    PPAP is a series of documents gathered in one specific location (a binder or electronically) called the "PPAP Package". The PPAP package is a series of documents which need a formal certification / sign-off by the supplier and approval / sign-off by the customer. The form that summarizes this package is called PSW (Part Submission Warrant).

  8. Regular Production Option - Wikipedia

    en.wikipedia.org/wiki/Regular_Production_Option

    The complete configuration of a GM vehicle (as it exited the factory) can be described by specifying the base model and a complete list of its RPO codes. [1] Some dealerships are willing to run a VIN and print out its RPOs (with their definitions) free of charge. The records are in GMs' electronic database since at least the 1990 models.

  9. On-board diagnostics - Wikipedia

    en.wikipedia.org/wiki/On-board_diagnostics

    GM's ALDL (Assembly Line Diagnostic Link) is sometimes referred to as a predecessor to, or a manufacturer's proprietary version of, an OBD-I diagnostic starting in 1981. . This interface was made in different varieties and changed with power train control modules (aka PCM, ECM, E