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In the 1980s, the European Union began harmonising regulatory requirements. In 1989, Europe, Japan, and the United States began creating plans for harmonisation. The International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) was created in April 1990 at a meeting in Brussels.
Synthetic: rayon, cellulose acetate, triacetate, natural rubber, nylon, polyester, polyurethanes; Metal: gold, silver, copper alloys; Decisions about appropriate textile stabilization are most effective when the fibers are identified. The primary method of determining a fiber type is through polarized light microscopy.
Textile fibres or textile fibers (see spelling differences) can be created from many natural sources (animal hair or fur, cocoons as with silk worm cocoons), as well as semisynthetic methods that use naturally occurring polymers, and synthetic methods that use polymer-based materials, and even minerals such as metals to make foils and wires.
Natural fibers are also used in composite materials, much like synthetic or glass fibers. These composites, called biocomposites, are a natural fiber in a matrix of synthetic polymers. [ 1 ] One of the first biofiber-reinforced plastics in use was a cellulose fiber in phenolics in 1908. [ 1 ]
United States: Although ICH GCP guidelines are recommended by the Food and Drug Administration (FDA), [4] they are not statutory in the United States. The National Institutes of Health requires NIH-funded clinical investigators and clinical trial staff who are involved in the design, conduct, oversight, or management of clinical trials to be ...
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.
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 ...
Dimensional stability (in fabric) pertains to a fabric's ability to maintain its initial size and shape even after undergoing wear and care, which is a desirable property. [1] Textile manufacturing is based on the conversion of fiber into yarn , yarn into fabric, includes spinning , weaving , or knitting , etc.