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  2. International Council for Harmonisation of Technical ...

    en.wikipedia.org/wiki/International_Council_for...

    The ICH topics are divided into four categories and ICH topic codes are assigned according to these categories: [11] Q: Quality Guidelines; S: Safety Guidelines; E: Efficacy Guidelines; M: Multidisciplinary Guidelines; ICH guidelines are not binding, and instead implemented by regulatory members through national and regional governance. [12]

  3. Textile stabilization - Wikipedia

    en.wikipedia.org/wiki/Textile_stabilization

    Coptic tunic tapestry fragment displaying characteristic physical deterioration that is treated through stabilization techniques. Textile stabilization is a conservation method for fiber and yarn-based cloth intended to mitigate damage, prevent degradation and preserve structural integrity.

  4. OECD Guidelines for the Testing of Chemicals - Wikipedia

    en.wikipedia.org/wiki/OECD_Guidelines_for_the...

    Section 5: Other Test Guidelines; Guidelines are numbered with three digit numbers, the section number being the first number. Sometimes guidelines are suffixed with a letter. Guidelines are under constant review, with guidelines being periodically updated, new guidelines being adopted, and guidelines being withdrawn.

  5. Stability testing (pharmaceutical) - Wikipedia

    en.wikipedia.org/wiki/Stability_testing...

    With stability testing, pharmaceutical industry inspects the quality of drug substances and drug products as per the guidelines outlined by US Food and Drug Administration and International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use to make sure that they retained the quality over the period of time.

  6. Trial master file - Wikipedia

    en.wikipedia.org/wiki/Trial_master_file

    The minimum essential documents that are required for the registration of pharmaceutical products designed for human use are specified in the document 'ICH Good Clinical Practices,' published in 1997 by the ICH [2] Example ICH essential documents that would be required in any US, EU or Japan based clinical trial would include: signed protocol ...

  7. Pharmacognosy - Wikipedia

    en.wikipedia.org/wiki/Pharmacognosy

    Pharmacognosy is the study of crude drugs obtained from medicinal plants, animals, fungi, and other natural sources. [1] The American Society of Pharmacognosy defines pharmacognosy as "the study of the physical, chemical, biochemical , and biological properties of drugs, drug substances, or potential drugs or drug substances of natural origin ...

  8. Natural fiber - Wikipedia

    en.wikipedia.org/wiki/Natural_fiber

    Natural fibers or natural fibres (see spelling differences) are fibers that are produced by geological processes, or from the bodies of plants or animals. [1] They can be used as a component of composite materials, where the orientation of fibers impacts the properties. [2] Natural fibers can also be matted into sheets to make paper or felt. [3 ...

  9. Pharmaceutical Inspection Convention and Pharmaceutical ...

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

    The PIC (Pharmaceutical Inspection Convention) was founded in October 1970 by the European Free Trade Association (EFTA), under the title of the Convention for the Mutual Recognition of Inspections in Respect of the Manufacture of Pharmaceutical Products.

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