Item no.
USP-RAPS-02
Unit
Each
Shipment details
No Dangerous Good
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Description
Many agencies around the world are tasked with regulating the healthcare product industry within their respective countries. These agencies and their suppliers require manufacturers to conduct internal audits of their quality management systems on a regular basis to ensure compliance with the appropriate standards and regulations. Without an effective audit program, a company is at higher risk for nonconformance, regulatory actions, security breaches, poor product quality, loss of certification and registration, increased product liability risk, and a suboptimal process improvement system.
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
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