[Webinar] USP Compliance: USP 795 Facility Requirements

October 4, 2019 Bryan Prince

Bryan Prince reviews the timeline for USP 795 compliance, QC processes for non-sterile compounding, staff training steps, and more.

Original content from Pharmacy Purchasing & Products - www.pppmag.com

About the Author

Bryan Prince, MBA is the owner and lead consultant at Lab·Red Pharmacy Consultants. His early career in containment technology allowed him access to pharmaceutical labs around the U.S. where he gleaned extensive knowledge of chemical handling technique and safety strategies. In 2012 he started visiting compounding pharmacies to observe workflow habits and share his knowledge, which led to writing articles for the International Journal of Pharmaceutical Compounding (IJPC). Bryan has been invited to speak at conferences on “Quality, Safety, and Workflow in the Compounding Pharmacy” for the American College of Apothecaries and PCCA. Most recently he has spoken on "Facility and Engineering Controls Using USP 800 Guidelines" for the ACA and IACP. He is also a contributor to the ACHC’s USP 800 education conferences and webinars.
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[Webinar] USP Compliance: USP 795 Facility Requirements

About the Author

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