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Ziprasidone Related Compound D

簡(jiǎn)要描述：

Ziprasidone Related Compound D

來(lái)源：英國(guó)政府化學(xué)家實(shí)驗(yàn)室該標(biāo)準(zhǔn)品提供科研實(shí)驗(yàn)

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更新時(shí)間：2024-09-09

 上海義森生物有限公司：Ziprasidone Related Compound D

美國(guó)USP標(biāo)準(zhǔn)簡(jiǎn)介：

The United States Pharmacopeial Convention （USP） is a scientific nonprofit organization that sets standards for the identity, strength, quality, and purity of medicines, food ingredients, and dietary supplements manufactured, distributed and consumed worldwide. USP’s drug standards are enforceable in the United States by the Food and Drug Administration, and these standards are developed and relied upon in more than 140 countries.

USP standards are developed and revised by more than 850 volunteer experts, including international participants, who work with USP under strict conflict-of-interest rules. Since its founding in 1820, USP has helped secure the quality of the American drug supply. Building on that legacy, USP today works with scientists, practitioners, and regulators of many nations to help protect public health worldwide.

 

 

 上海義森生物有限公司：Ziprasidone Related Compound D

USP里程碑

 

Milestone of 3,000 USP Reference Standards
Public Health Supported by Breadth of Quality Standards
Rockville, Md., March 5, 2013 — In a milestone representing a significant contribution to public health, the U.S. Pharmacopeial Convention （USP） announces that it has grown its portfolio of reference standards to now include 3,000 items. USP Reference Standards are highly characterized samples of active pharmaceutical ingredients and impurities, food chemicals, and dietary supplements and their ingredients. Regulators and manufacturers use USP Reference Standards to assess products’ conformity to standards of identity, quality, purity and strength. USP Reference Standards are specified in the monographs of the U.S. Pharmacopeia and National Formulary （USP–NF）, USP’s flagship compendia of quality standards; the Food Chemicals Codex （for food ingredients）, the Dietary Supplements Compendium, and the new Medicines Compendium. Drugs sold or manufactured in the United States are required by law to comply with standards published in the USP–NF, and these standards are enforceable by the Food and Drug Administration.
“Attaining 3,000 USP Reference Standards is important for USP, of course, but also for all stakeholders interested in advancing public health,” said Roger L. Williams, M.D., chief executive officer at USP. “USP relies on our volunteer experts who, with staff, set the standards, and on the manufacturers who donate the monographs and materials from which many of our standards are derived. Both are equally crucial in the standards-setting process, and I want to take this opportunity to thank all who understand the importance of public standards.”
Dr. Williams also noted USP’s focused effort over the last decade to strengthen USP’s public standards. This effort is ongoing, and is summarized in USP’s policy statements and in a stimuli article.
USP distributes thousands of units of its Reference Standards every year to customers in more than 140 countries around the world. The breadth and depth of the USP catalog means that regulators and manufacturers have the fullest available complement of publicly available standards to help ensure the quality of medicines, foods and dietary supplements throughout the supply chain, from manufacturers to practitioners, patients and consumers.

 

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