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  2. Biomedical equipment technician - Wikipedia

    en.wikipedia.org/wiki/Biomedical_Equipment...

    All three forces remain in rigorous, tri-service training for 10 months prior to returning to their individual services. The training is held at Fort Sam Houston and is a part of the Medical Education and Training Campus (METC).The first METC BMET class started on August 4, 2010, and the last Sheppard class graduated on January 14, 2011. [16]

  3. Aseptic processing - Wikipedia

    en.wikipedia.org/wiki/Aseptic_processing

    Equipment used in aseptic processing of food and beverages must be sterilized before processing and remain sterile during processing. [1] When designing aseptic processing equipment there are six basic requirements to consider: the equipment must have the capability of being cleaned thoroughly, it must be able to be sterilized with steam, chemicals, or high-temperature water, sterilization ...

  4. Healthcare Sterile Processing Association - Wikipedia

    en.wikipedia.org/wiki/Healthcare_Sterile...

    The Healthcare Sterile Processing Association (HSPA), formerly International Association of Health Central Service Material Management (IAHSCMM), [3] is a professional association which represents healthcare Central Service (CS) professionals, and is based in Chicago, Illinois with over 48,000 [4] members worldwide.

  5. Central sterile services department - Wikipedia

    en.wikipedia.org/wiki/Central_sterile_services...

    Sterile dental instruments from hospital central supply (barcoded label indicating sterilization date, expiry date and contents). The central sterile services department (CSSD), also called sterile processing department (SPD), sterile processing, central supply department (CSD), or central supply, is an integrated place in hospitals and other health care facilities that performs sterilization ...

  6. ISO 13485 - Wikipedia

    en.wikipedia.org/wiki/ISO_13485

    ISO 13485 Medical devices -- Quality management systems -- Requirements for regulatory purposes is a voluntary standard, [1] published by International Organization for Standardization (ISO) for the first time in 1996, and contains a comprehensive quality management system for the design and manufacture of medical devices.

  7. Autoclave - Wikipedia

    en.wikipedia.org/wiki/Autoclave

    Cutaway illustration of a cylindrical-chamber autoclave. An autoclave is a machine used to carry out industrial and scientific processes requiring elevated temperature and pressure in relation to ambient pressure and/or temperature.

  8. Blow fill seal - Wikipedia

    en.wikipedia.org/wiki/Blow_fill_seal

    BFS-packaged eye drops for single use. Blow-Fill-Seal, also spelled as Blow/Fill/Seal, in this article abbreviated as BFS, is an automated manufacturing process by which plastic containers, such as bottles or ampoules are, in a continuous operation, blow-formed, filled, and sealed.

  9. Cleanroom - Wikipedia

    en.wikipedia.org/wiki/Cleanroom

    Cleanroom from outside Entrance to a cleanroom with no air shower Cleanroom for microelectronics manufacturing with fan filter units installed in the ceiling grid Cleanroom cabin for precision measuring tools Typical cleanroom head garment. A cleanroom or clean room is an engineered space that maintains a very low concentration of airborne ...

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