Jump to content
 







Main menu
   


Navigation  



Main page
Contents
Current events
Random article
About Wikipedia
Contact us
Donate
 




Contribute  



Help
Learn to edit
Community portal
Recent changes
Upload file
 








Search  

































Create account

Log in
 









Create account
 Log in
 




Pages for logged out editors learn more  



Contributions
Talk
 



















Contents

   



(Top)
 


1 History of the United States Pharmacopeia Organization  





2 Product qualitystandards and verification  





3 Healthcare information  





4 Promoting the Quality of Medicines program  





5 International agreements and offices  





6 See also  





7 References  





8 External links  














United States Pharmacopeia






العربية
Eesti
Español
Français

Bahasa Indonesia
Nederlands
Português

Tiếng Vit

 

Edit links
 









Article
Talk
 

















Read
Edit
View history
 








Tools
   


Actions  



Read
Edit
View history
 




General  



What links here
Related changes
Upload file
Special pages
Permanent link
Page information
Cite this page
Get shortened URL
Download QR code
Wikidata item
 




Print/export  



Download as PDF
Printable version
 
















Appearance
   

 





Coordinates: 39°0348N 77°0656W / 39.063270°N 77.115574°W / 39.063270; -77.115574
 

From Wikipedia, the free encyclopedia
 

(Redirected from U.S. Pharmacopeia)

United States Pharmacopeia
Company typeNonprofit
Founded1820; 204 years ago (1820)
Headquarters ,
United States

Key people

Ronald T. Piervincenzi (CEO)[1]
Websitewww.usp.org

The United States Pharmacopeia (USP) is a pharmacopeia (compendium of drug information) for the United States published annually by the over 200-year old United States Pharmacopeial Convention (usually also called the USP), a nonprofit organization that owns the trademark and also owns the copyright on the pharmacopeia itself.

The USP is published in a combined volume with the National Formulary (aformulary) 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". Drugs subject to USP standards include both human drugs (prescription, over-the-counter, or otherwise) and animal drugs. USP-NF standards also have a role in US federal law; a drug or drug ingredient with a name recognized in USP-NF is considered adulterated if it does not satisfy compendial standards for strength, quality, or purity. USP also sets standards for dietary supplements and food ingredients (as part of the Food Chemicals Codex). USP has no role in enforcing its standards; enforcement is the responsibility of the U.S. Food and Drug Administration (FDA) and other government authorities in the United States.[vague][citation needed]

History of the United States Pharmacopeia Organization

[edit]

The U.S. Pharmacopeia (USP) was formed in 1820 when 11 physicians came together to take action to protect patients from being harmed by the inconsistent and poor-quality medical preparations at that time. The first standards were "recipes" that guided the preparation of medicines, which were often manufactured in apothecaries relying heavily on crude botanical drugs having therapeutic activities.[3] When the modern pharmaceutical industry emerged, USP standards changed from those "recipes" to a set of quality specifications for medicines along with analytical tests to be performed to assess their purity, quality, and authenticity.[3]

Product quality–standards and verification

[edit]

USP establishes documentary (written) and reference (physical) standards for medicines, food ingredients, dietary supplement products, and ingredients. These standards are used by regulatory agencies and manufacturers to help to ensure that these products are of the appropriate identity, as well as strength, quality, purity, and consistency. USP 800 is an example of a publication created by the United States Pharmacopeia.

Prescription and over-the-counter medicines available in the United States must, by federal law, meet USP-NF public standards, where such standards exist. Many other countries use the USP-NF instead of issuing their own pharmacopeia, or to supplement their government pharmacopeia.

USP's standards for food ingredients can be found in its Food Chemicals Codex (FCC). The FCC is a compendium of standards used internationally for the quality and purity of food ingredients like preservatives, flavorings, colorings, and nutrients. While the FCC is recognized in law in countries like Australia, Canada, and New Zealand, it currently does not have statutory recognition in the United States, although FCC standards are incorporated by reference in over 200 FDA food regulations.[4] USP obtained the FCC from the Institute of Medicine in 2006. The IOM had published the first five editions of the FCC.

USP also conducts verification programs for dietary supplement products and ingredients. These are testing and audit programs. Products that meet the requirements of the program can display the USP Verified Dietary Supplement Mark on their labels.[5] This is different from seeing the letters "USP" alone on a dietary supplement label, which means that the manufacturer is claiming to adhere to USP standards. USP does not test such products as it does with USP Verified products.

Healthcare information

[edit]

In the past, Congress authorized the Secretary of HHS to request USP to develop a drug classification system that Medicare Prescription Drug Benefit plans may use to develop their formularies,[6] and to revise such classification from time to time to reflect changes in therapeutic uses covered by Part D drugs and the addition of new covered Part D drugs. USP has developed six versions of the Model Guidelines, the last issued early in 2014 for the 2015–2017 benefit years.[7]

Promoting the Quality of Medicines program

[edit]

Since 1992, USP has worked cooperatively with the United States Agency for International Development (USAID) to help developing countries address critical issues related to poor quality medicines. This partnership operated as the Drug Quality and Information (DQI) program until 2009, when, to better meet growing global needs, USAID awarded USP a five-year, $35 million cooperative agreement to establish a new, expanded program called Promoting the Quality of Medicines (PQM).[8][9] In 2013 USAID extended the PQM program for five years (through September 2019), increased its funding to $110 million, and expanded the geographical reach of the program.[10]

PQM serves as a primary mechanism to help USAID-supported countries strengthen their quality assurance and quality control systems to better ensure the quality of medicines that reach patients. PQM has four key objectives:[11]

USP-USAID collaborative efforts have helped communities improve drug quality in more than 35 countries. PQM currently works in Africa,[12] Asia,[13] Europe/Eurasia,[14] and the Caribbean/Latin America.[15]

International agreements and offices

[edit]

USP works internationally, largely through agreements with other pharmacopeias, as well as regulatory bodies, manufacturer associations, and others. In recent years, USP signed a series of Memoranda of Understanding (MOU) with groups including the Pharmacopeia of the People's Republic of China Chinese Pharmacopeia Commission, nine countries belonging to the Association of Southeast Asian Nations (ASEAN), and the Federal Service on Surveillance in Healthcare and Social Development of the Russian Federation (Roszdravnadzor).[16] USP also operates an international office in Switzerland and offices and laboratories in Brazil, India, and China.

See also

[edit]
  • British Pharmacopoeia
  • European Pharmacopoeia
  • Japanese Pharmacopoeia
  • Pharmacopoeia of the People's Republic of China
  • The International Pharmacopoeia
  • National formulary
  • Food and Drug Administration
  • Genome Valley
  • Pharmacopeia
  • Pill splitting, for a discussion of USP standards concerning the uniformity of dosage
  • USP 800
  • References

    [edit]
    1. ^ U.S. Pharmacopeial Convention (2014-01-08), "Ron Piervincenzi, Ph.D., Named Next CEO Of USP", PR Newswire
  • ^ "National Formulary". MedicineNet. Retrieved 2015-12-11.
  • ^ a b "U.S. Pharmacopeia: Building trust for 200 years". Archived from the original on 2023-05-18. Retrieved 2023-08-18.
  • ^ "Federal Register | Food Additive Regulations; Incorporation by Reference of the Food Chemicals Codex, 7th Edition". www.federalregister.gov. Retrieved 2015-12-11.
  • ^ "Are Dietary Supplements Dangerous? - Consumer Reports". www.consumerreports.org. Retrieved 2015-12-11.
  • ^ "United States Pharmacopeia (USP). Medicare Prescription Drug Benefit Model Guidelines Source Information". www.nlm.nih.gov. Retrieved 2015-12-11.
  • ^ webadmin. "Part D Model Guidelines Updated Far Too Infrequently". Managed Care Magazine Online. Retrieved 2015-12-11.
  • ^ "Promoting the Quality of Medicines (PQM)".
  • ^ "How to curb 'fake' food, drug products in Nigeria by PQM". www.ngrguardiannews.com. 6 August 2015. Retrieved 2015-12-11.
  • ^ "USAID extends USP's Promoting the Quality of Medicines (PQM) programme - Express Pharma Online". archivepharma.financialexpress.com. Retrieved 2015-12-11.
  • ^ "Promoting the Quality of Medicines (PQM)". www.usp.org. Retrieved 2015-12-11.
  • ^ "PQM Activities in Africa | U.S. Pharmacopeial Convention". United States Pharmacopoeia. Archived from the original on 2016-04-05.
  • ^ "PQM Accomplishments in Asia | U.S. Pharmacopeial Convention". United States Pharmacopoeia. Archived from the original on 2016-04-08.
  • ^ "PQM in Europe-Eurasia | U.S. Pharmacopeial Convention". United States Pharmacopoeia. Archived from the original on 2016-04-05.
  • ^ "PQM's Work in Latin America and the Caribbean | U.S. Pharmacopeial Convention". United States Pharmacopoeia. Archived from the original on 2016-04-05.
  • ^ Федеральная служба по надзору в сфере здравоохранения
  • [edit]

    39°03′48N 77°06′56W / 39.063270°N 77.115574°W / 39.063270; -77.115574


    Retrieved from "https://en.wikipedia.org/w/index.php?title=United_States_Pharmacopeia&oldid=1171083387"

    Categories: 
    Companies based in Rockville, Maryland
    American medical research
    Pharmacopoeias
    Hidden categories: 
    Pages using gadget WikiMiniAtlas
    Articles with short description
    Short description is different from Wikidata
    Articles with a promotional tone from August 2022
    All articles with a promotional tone
    All Wikipedia articles needing clarification
    Wikipedia articles needing clarification from April 2019
    All articles with unsourced statements
    Articles with unsourced statements from April 2019
    Articles with ISNI identifiers
    Articles with VIAF identifiers
    Articles with J9U identifiers
    Articles with LCCN identifiers
    Articles with SUDOC identifiers
    Coordinates not on Wikidata
     



    This page was last edited on 18 August 2023, at 23:25 (UTC).

    Text is available under the Creative Commons Attribution-ShareAlike License 4.0; additional terms may apply. By using this site, you agree to the Terms of Use and Privacy Policy. Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc., a non-profit organization.



    Privacy policy

    About Wikipedia

    Disclaimers

    Contact Wikipedia

    Code of Conduct

    Developers

    Statistics

    Cookie statement

    Mobile view



    Wikimedia Foundation
    Powered by MediaWiki