Revisions next stage free#

The following USP RS, which were not available when the associated monograph was made official, have since become available.

New USP Reference Standards (updated as of July 24, 2020).

Click here to subscribe to our newsletter, The Standard, to receive a monthly snapshot of new and updated RS's. Visit the USP Reference Standards Catalog and the online USP Store for a complete listing of available USP RS's and to obtain RS documentation (e.g., USP Certificates, SDS), lot validity, and more. Lists of 'New USP Reference Standards' and 'Unavailable First-time Official USP Reference Standards' are provided below. Learn more about the harmonization process by visiting the Harmonization-Pharmacopeial Discussion Group section of USP's website. View current Notices of Stage 4 Harmonization. Stage 6 adopted text is published so that USP–NF users may become aware of its availability as a pharmacopeial standard and its targeted official date. Harmonization Stage 4 includes monographs or general chapters that have completed stages 1-4 of the pharmacopeial harmonization process resulting in approved USP–NF text.

Revisions next stage free#

To receive periodic email updates when USP posts New Official Text, sign up for the free Compendial Updates service. Learn more by visiting the Accelerated Revision History and the USP Guideline on Use of Accelerated Processes for Revisions to the USP–NF. Once published in the print and online publications, Revision Bulletins and IRAs are official as of the date indicated on the website and are not subject to the general six-month delayed official date for the particular publication. Errata are incorporated into the next available official publication. Errata are posted on the Web site and are official the first day of the following month. Errata are considered to be text erroneously published in the USP–NF that does not accurately reflect the intended requirements as approved by the Council of Experts.IRAs are incorporated into the next available official publication. Like Revision Bulletins, IRAs supersede standards published in the print and online USP–NF. Once comments (if any) are reviewed and the IRA is approved by the appropriate Expert Committee, final IRAs are posted on the USP website. IRAs are proposed in PF for a 90-day public comment period.A Revision Bulletin posted on the USP website indicates its posting date and official date. Revision Bulletinsare USP's most expedited revisions and supersede standards published in the USP–NF (print and online versions).

Accelerated Revisions: Revision Bulletins, IRAs, & Errata Accelerated Revisions include Revision Bulletins, Interim Revision Announcements (IRAs), and Errata.

USP uses its Accelerated Revision processes to expedite revisions to the USP–NF. Revisions are presented three times a year in the USP-NF as Issues 1, 2, and 3, and as monthly Accelerated Revisions on the USP website. The United States Pharmacopeia–National Formulary ( USP–NF) is continuously revised. USP–NF's Continuous Revision Process and Superseded Text