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Description

Medication misuse has resulted in more than 1 million adverse drug events per year in the United States. Patients’ best source (and often only source) of information regarding the medications they have been prescribed is on the prescription container label. Although other written information and oral counseling sometimes may be available, the prescription container label must fulfill the professional obligations of the prescriber and pharmacist. These obligations include giving the patient the most essential information needed to understand how to safely and appropriately use the medication and to adhere to the prescribed medication regimen. This 90-minute webinar will cover the definition and purpose of USP Chapter <17> for prescription container labeling standards, an overview of the logic for this chapter, prescription labeling issues, and the relevant state regulations available. Furthermore, it explores the key concepts of USP General Chapter <17> on labeling along with the latest update for this chapter and future directions.

Miscellaneous

Certificate of Analysis (specimen)

Reference Material CoA specimen: for the current lot, please contact your customer service representative at info@labmix24.com

Product data sheet

View all available product details e.g. description, analytes/parameters, CAS Number, concentrations/values, sales unit/product format, method, source, transport information

USP | United States Pharmacopeia

US Pharmacopeia Standards set a global benchmark, enabling efficient, reliable, and cost-effective development and quality control of pharmaceuticals.

Official USP Reference Standards are highly characterized physical specimens intended for quality control use when conducting assays and tests for medicines as described in the USP-NF. When you conduct tests and assays required by the USP-NF using the USP reference standards specified, the results can be considered conclusive.

As a USP-Authorized Distributor, we offer the following products and services:

  • USP Reference Standards
  • USP Pharmaceutical Analytical Impurities
  • USP Training and educational programs