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  2. United States Pharmacopeia - Wikipedia

    en.wikipedia.org/wiki/United_States_Pharmacopeia

    The USP is published in a combined volume with the National Formulary (a formulary) as the USP-NF. [2] If a drug ingredient or drug product has an applicable USP quality standard (in the form of a USP-NF monograph), it must conform in order to use the designation "USP" or "NF".

  3. Pharmaceutical Inspection Convention and Pharmaceutical ...

    en.wikipedia.org/wiki/Pharmaceutical_Inspection...

    The Pharmaceutical Inspection Convention and Pharmaceutical Inspection Co-operation Scheme (PIC/S) are two international instruments between countries and pharmaceutical inspection authorities. The PIC/S is meant as an instrument to improve co-operation in the field of Good Manufacturing Practices between regulatory authorities and the ...

  4. 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]

  5. Visual inspection - Wikipedia

    en.wikipedia.org/wiki/Visual_inspection

    Visual inspection is a common method of quality control, data acquisition, and data analysis.Visual Inspection, used in maintenance of facilities, mean inspection of equipment and structures using either or all of raw human senses such as vision, hearing, touch and smell and/or any non-specialized inspection equipment.

  6. Form FDA 483 - Wikipedia

    en.wikipedia.org/wiki/Form_FDA_483

    The header identifies the FDA district office that performed the inspection, the date(s) of inspection, name and address of the facility that was inspected, the name and title of the individual to whom the 483 is issued to (usually the most responsible individual physically present in the facility), a brief description of the type of facility, and the facility's FEI (FDA Establishment ...

  7. Suspect in Germany auto attack that killed 5 self-identified ...

    www.aol.com/news/suspect-germany-auto-attack...

    The suspect in the German car-ramming attack that killed five and injured more than 200 on Friday has been identified as Taleb al-Abdulmohsen, a self-described member of the “liberal opposition ...

  8. USP 800 - Wikipedia

    en.wikipedia.org/wiki/USP_800

    USP 800 (Hazardous Drugs—Handling in Healthcare Settings) is a guideline created by the United States Pharmacopeia Convention (USP), as one of their General Chapters through which the USP "sets quality standards for medicines, dietary supplements and food ingredients".

  9. Patent Act of 1790 - Wikipedia

    en.wikipedia.org/wiki/Patent_Act_of_1790

    Hopkins left behind a series of manuscripts describing the utility of his discovery of Potash, which is derived from a crude form of potassium carbonate and may be deemed as one of America's first chemicals to become widely used in industrial fields. The third patent was granted to a man named Oliver Evans on December 18, 1790. This patent ...