Item no.
USP-DS-GMP-02
Unit
Each
Shipment details
No Dangerous Good
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Description
This course will focus on key aspects and approaches for QC operations to comply with the dietary supplement GMP requirements, and on the use and benefits of USP monographs, test procedures, Reference Standards, and general guidance chapters to help meet GMP compliance. The course will also cover GMP compliance for QC laboratory operations, covering a broad range of topics, including specifications for components and finished products, analytical instrument qualification and calibration, validation and verification of test procedures, and internal and third-party laboratory audits. The live version of this webcast took place on June 2, 2016. (Webcast 6 hours 11 minutes)
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