USP <797> Overview
In this video, Matt Martin, PharmD, provides a comprehensive overview of proposed changes to USP Chapter <797> prior to publication of the chapter on June 1, 2019.
USP <797> Webinar
Matt Martin, PharmD, and Ross Caputo, PhD, shared detailed information about how the 2019 revisions to USP <797> affect your personnel qualifications, facilities and documentation. This webinar provides assistance to pharmacies that compound sterile preparations.
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Notable Changes in the New USP <797>
Dylan Herr, RA/QA Development Manager at Eagle, understands that the revised USP <797> chapter for sterile compounding makes significant revisions to the old chapter. In this latest article, Dyan is happy to provide you with an overview of those changes and strategies for implementing them.
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ScanRDI® Sterility Test Protocol
A faster way to comply with USP <797> and ensure your patients are receiving quality compounds, the ScanRDI can deliver results in as little as one business day, and it fulfills the method suitability requirement as outlined in USP <1223>.
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USP
USP General Chapter <797> Pharmaceutical Compounding – Sterile Preparations
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