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Description

This course of the education offering is meant for Institution (Hospital) Leaders responsible for the understanding, support and implementation of USP standards on compounding (General Chapters <797> and <795>) and safe handling of hazardous drugs (General Chapter <800>).<br>The course for Institution Leaders defines the roles and responsibilities of hospital leadership regarding the implementation and compliance with USP General Chapters <795>, <797> and <800> and describes the quality, regulatory and reimbursement impact of compliance with USP standards on healthcare organizations.

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