Item no.
USP-CM-1029-02
Unit
Each
Shipment details
No Dangerous Good
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Description
Good Documentation Practices is an essential element in regulated manufacturing and laboratory environments. Personnel in these fields need to closely adhere to GDP in order to ensure an auditable account of work performed. GDP is required for all documentation included in a fully developed quality system. This self-paced e-learning course will cover all aspects of GDP, including practices for writing and correcting documentation as well as the various documentation and record keeping requirements as per the US FDA CFR sections (21 CFR 11, 58, 211, 312, 812), EU regulations, and ICH guidelines, as applicable to non-clinical laboratory studies, pharmaceuticals and medical device.
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