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  2. United States Pharmacopeia - Wikipedia

    en.wikipedia.org/wiki/United_States_Pharmacopeia

    Products that meet the requirements of the program can display the USP Verified Dietary Supplement Mark on their labels. [5] This is different from seeing the letters "USP" alone on a dietary supplement label, which means that the manufacturer is claiming to adhere to USP standards. USP does not test such products as it does with USP Verified ...

  3. Tablet hardness testing - Wikipedia

    en.wikipedia.org/wiki/Tablet_hardness_testing

    Tablet hardness testing is a laboratory technique used by the pharmaceutical industry to determine the breaking point and structural integrity of a tablet and find out how it changes "under conditions of storage, transportation, packaging and handling before usage" [1] The breaking point of a tablet is based on its shape. [2]

  4. Chemical purity - Wikipedia

    en.wikipedia.org/wiki/Chemical_purity

    USP grade meets the purity levels set by the United States Pharmacopeia (USP). USP grade is equivalent to the ACS grade for many drugs. NF grade is a purity grade set by the National Formulary (NF). NF grade is equivalent to the ACS grade for many drugs. British Pharmacopoeia: Meets or exceeds requirements set by the British Pharmacopoeia (BP ...

  5. Bioburden - Wikipedia

    en.wikipedia.org/wiki/Bioburden

    21 C.F.R. 211.110 (a)(6) states that bioburden in-process testing must be conducted pursuant to written procedures during the manufacturing process of drug products. [3] The United States Pharmacopeia (USP) outlines several tests that can be done to quantitatively determine the bioburden of non-sterile drug products. [4]

  6. Dissolution testing - Wikipedia

    en.wikipedia.org/wiki/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. Design for testing - Wikipedia

    en.wikipedia.org/wiki/Design_for_testing

    DFT affects and depends on the methods used for test development, test application, and diagnostics. Most tool-supported DFT practiced in the industry today, at least for digital circuits, is predicated on a Structural test paradigm. Structural test makes no direct attempt to determine if the overall functionality of the circuit is correct.

  8. Test management tool - Wikipedia

    en.wikipedia.org/wiki/Test_management_tool

    Test management tools offer the prospect of streamlining the testing process and allow quick access to data analysis, collaborative tools and easy communication across multiple project teams. Many test management tools incorporate requirements management capabilities to streamline test case design from the requirements. Tracking of defects and ...

  9. United States Patent and Trademark Office - Wikipedia

    en.wikipedia.org/wiki/United_States_Patent_and...

    The site also provides Boolean search and analysis tools. [99] The USPTO's free distribution service only distributes the patent documents as a set of TIFF files. [100] Numerous free and commercial services provide patent documents in other formats, such as Adobe PDF and CPC.