The United
States Pharmacopeia (USP) has a long history dating back to 1820, when a group
of physicians and pharmacists established the first edition of the USP to
promote standardization and quality of drugs in the United States. Over the
years, the USP has evolved into a comprehensive compendium of monographs that
provide specifications for the identity, strength, purity, and quality of
medicines, dietary supplements, and healthcare products.
In 1906, the
Pure Food and Drug Act was passed, which gave the USP official recognition by
the U.S. government. The USP became an official compendium of drug standards,
and its standards were used by regulatory agencies to enforce the law.
Over the
years, the USP has continued to update and revise its standards to reflect
advances in science and technology. In 1975, the USP merged with the
National Formulary (NF) to become the USP-NF, which included monographs
for both drugs and excipients.
Today, the
USP continues to play a critical role in promoting the quality and safety of
medicines and other healthcare products in the United States and around the
world. Its standards are widely used by manufacturers, regulatory agencies, and
other stakeholders to ensure that products are of high quality and safe for use
by consumers.
United
States Pharmacopeia (USP) has an online presence where you can access their
standards, publications, and resources. You can visit their website at www.usp.org to learn more about their mission and activities, and to access their
online compendium of monographs known as the USP-NF. The website also provides
information on USP's testing and verification services, accreditation programs,
and educational offerings. Additionally, there are online tools and resources
available to help manufacturers, healthcare professionals, and consumers ensure
that medicines and healthcare products are of high quality and safe to use.
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