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  2. Medical materiel - Wikipedia

    en.wikipedia.org/wiki/Medical_materiel

    In addition, medical supply technicians are responsible for maintaining requirements and records on storage/war reserve materiel; establishing stock control levels and inventory control; controlled medical items (i.e. drugs and precious metals); and delivering supplies and equipment to the customers. Medical logistics is often confused with and ...

  3. Central sterile services department - Wikipedia

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

    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 and other actions on medical devices, equipment and consumables; for subsequent ...

  4. Biomedical waste - Wikipedia

    en.wikipedia.org/wiki/Biomedical_waste

    Many healthcare facilities routinely use an autoclave to sterilize medical supplies. If the same autoclave is used to sterilize supplies and treat biomedical waste, administrative controls must be used to prevent the waste operations from contaminating the supplies. Effective administrative controls include operator training, strict procedures ...

  5. Medical Stores Department - Wikipedia

    en.wikipedia.org/wiki/Medical_Stores_Department

    Medical Stores Department (MSD) was established by the Act of Parliament No.13 of 1993 as an autonomous department under the Ministry of Health, Social Development, Gender, Elderly and Children responsible for develop, maintain and manage an efficient and cost effective system of procurement, storage and distribution of approved medicines and medical supplies required for use by the public ...

  6. Package testing - Wikipedia

    en.wikipedia.org/wiki/Package_testing

    Packaging for medical materials, medical devices, health care supplies, etc., have special user requirements and is highly regulated. Barrier properties, durability, visibility, sterility and strength need to be controlled; usually with documented test results for initial designs and for production.

  7. Good documentation practice - Wikipedia

    en.wikipedia.org/wiki/Good_documentation_practice

    Good documentation practice (recommended to abbreviate as GDocP to distinguish from "good distribution practice" also abbreviated GDP) is a term in the pharmaceutical and medical device industries to describe standards by which documents are created and maintained.