enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. USP Controlled Room Temperature - Wikipedia

    en.wikipedia.org/wiki/USP_Controlled_Room...

    The USP Controlled Room Temperature is a series of United States Pharmacopeia guidelines for the storage of pharmaceuticals; [1] the relevant omnibus standard is USP 797. [2] [3] Although 100% compliance remains challenging for any given facility, [4] the larger protocol may be regarded as constituting a form of clean room [5] which is included in a suite of best practices.

  3. Bioburden - Wikipedia

    en.wikipedia.org/wiki/Bioburden

    Contact plates or sterile swabs can also be used to test for microbes on a surface when compounding sterile products to ensure compliance with USP 797. [ 5 ] As an alternative to traditional methods (membrane-filtration and plate count method) there are rapid microbiological methods (RMM) that correlate to plate counting and give results in ...

  4. United States Pharmacopeia - Wikipedia

    en.wikipedia.org/wiki/United_States_Pharmacopeia

    USP establishes documentary (written) and reference (physical) standards for medicines, food ingredients, dietary supplement products, and ingredients. These standards are used by regulatory agencies and manufacturers to help to ensure that these products are of the appropriate identity, as well as strength, quality, purity, and consistency.

  5. Rubbing alcohol - Wikipedia

    en.wikipedia.org/wiki/Rubbing_alcohol

    All rubbing alcohols are volatile and flammable.Ethyl rubbing alcohol has an extremely bitter taste from additives. The specific gravity of Formula 23-H is between 0.8691 and 0.8771 at 15.56 °C (60.01 °F).

  6. Terminal cleaning - Wikipedia

    en.wikipedia.org/wiki/Terminal_cleaning

    Nosocomial infections claim approximately 90,000 lives in the United States annually. When patients are hospitalized and identified as having methicillin-resistant Staphylococcus aureus or infections that can be spread to other patients, best practices isolate these patients in rooms that are subjected to terminal cleaning when the patient is discharged.

  7. Cleaning validation - Wikipedia

    en.wikipedia.org/wiki/Cleaning_validation

    Cleaning validation is the methodology used to assure that a cleaning process removes chemical and microbial residues of the active, inactive or detergent ingredients of the product manufactured in a piece of equipment, the cleaning aids utilized in the cleaning process and the microbial attributes.

  8. Sodium dichloroisocyanurate - Wikipedia

    en.wikipedia.org/wiki/Sodium_dichloroisocyanurate

    Sodium dichloroisocyanurate (INN: sodium troclosene, troclosenum natricum or NaDCC or SDIC) is a chemical compound widely used as a cleansing agent and disinfectant. [1] It is a colorless, water-soluble solid, produced as a result of reaction of cyanuric acid with chlorine. The dihydrate is also known as is the potassium salt .

  9. List of cleaning products - Wikipedia

    en.wikipedia.org/wiki/List_of_cleaning_products

    This is a list of cleaning products and agents. Cleaning agents are substances (usually liquids, powders, sprays, or granules) used to remove dirt, including dust, stains, bad smells, and clutter on surfaces. Purposes of cleaning agents include health, beauty, removing offensive odor, and avoiding the spread of dirt and contaminants to oneself ...