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  2. Cleanroom - Wikipedia

    en.wikipedia.org/wiki/Cleanroom

    The ambient outdoor air in a typical urban area contains 35,000,000 particles for each cubic meter in the size range 0.5 μm and bigger, equivalent to an ISO 9 certified cleanroom. By comparison, an ISO 14644 -1 level 1 certified cleanroom permits no particles in that size range, and just 12 particles for each cubic meter of 0.3 μm and smaller.

  3. USP Controlled Room Temperature - Wikipedia

    en.wikipedia.org/.../USP_Controlled_Room_Temperature

    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.

  4. Room temperature - Wikipedia

    en.wikipedia.org/wiki/Room_temperature

    Retrieved 4 April 2018. 1.2.3.3 Definition of Room Temperature: According to the United States Pharmacopeia National Forumlary [ sic] (USP-NF), the definition of room temperature is between 15 and 30 °C in the United States. However, in the EU, the room temperature is defined as being 15 to 25 °C, while in Japan, it is defined being 1 to 30 °C.

  5. Operating temperature - Wikipedia

    en.wikipedia.org/wiki/Operating_temperature

    An operating temperature is the allowable temperature range of the local ambient environment at which an electrical or mechanical device operates. The device will operate effectively within a specified temperature range which varies based on the device function and application context, and ranges from the minimum operating temperature to the maximum operating temperature (or peak operating ...

  6. Dissolution testing - Wikipedia

    en.wikipedia.org/wiki/Dissolution_testing

    Dissolution testing. In the pharmaceutical industry, drug dissolution testing is routinely used to provide critical in vitro drug release information for both quality control purposes, i.e., to assess batch-to-batch consistency of solid oral dosage forms such as tablets, and drug development, i.e., to predict in vivo drug release profiles. [ 1]

  7. Cold chain - Wikipedia

    en.wikipedia.org/wiki/Cold_chain

    v. t. e. Cold chain is a set of rules and procedures that ensure the systematic coordination of activities for ensuring temperature-control of goods while in storage and transit. The objective of a cold chain is to preserve the integrity and quality of goods such as pharmaceutical products or perishable good from production to consumption. [ 1 ...

  8. Room-temperature superconductor - Wikipedia

    en.wikipedia.org/wiki/Room-temperature...

    A room-temperature superconductor is a hypothetical material capable of displaying superconductivity above 0 °C (273 K; 32 °F), operating temperatures which are commonly encountered in everyday settings. As of 2023, the material with the highest accepted superconducting temperature was highly pressurized lanthanum decahydride, whose ...

  9. United States Pharmacopeia - Wikipedia

    en.wikipedia.org/wiki/United_States_Pharmacopeia

    www .usp .org. The United States Pharmacopeia ( USP) is a pharmacopeia (compendium of drug information) for the United States published annually by the over 200-year old United States Pharmacopeial Convention (usually also called the USP), a nonprofit organization that owns the trademark and also owns the copyright on the pharmacopeia itself.