Item no.
USP-HQS-797-01
Unit
Each
Shipment details
No Dangerous Good
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Description
This full-day course discusses key sterile compounding standards in USP General Chapter <797> Pharmaceutical Compounding-Sterile Preparations. The course will describe the scope and purpose of USP <797>, the microbial contamination risk levels, and methods of sterilization. The course will describe the facility and engineering control requirements for the sterile compounding areas as well as the environmental monitoring requirements. The course will outline the personnel training, garbing, and assessment requirements and the quality control and quality assurance processes to ensure quality compounded preparations.
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
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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