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Bryan Prince, Lab-Red Pharmacy Consultants

Bryan Prince

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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More by This Author

Primary Engineering Control Placement in the Cleanroom

Primary Engineering Control Placement in the Cleanroom

This white paper explores PEC selection and placement strategies to meet USP <797> and <800> guidelines in cleanrooms handling sterile and hazardous drug compounding.

USP Compliance: USP 795 Facility Requirements Webinar

USP Compliance USP 795 Facility Requirements

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

PEC and C-PEC Installation Process

PEC and C-PEC Installation Process

Discover the intricacies of installing Primary Engineering Controls (PECs) and Containment Primary Engineering Controls (C-PECs) in a pharmacy setting through our insightful white paper authored by Bryan Prince.

Improve Workflow with Cleanroom Design White Paper

Improve Workflow with Cleanroom Design

<p>This white paper discusses 503A pharmacy requirements and USP chapters <797> and <800> as it relates to cleanroom design.</p>

Facility and Engineering Controls Using USP 800 Guidelines

The focus of this article is to discuss the details for consideration of a good working design of a USP 800 compliant compounding lab.

Engineering Control Options Under USP 800

Engineering Control Options Under USP 800

Explore USP 800 engineering controls in our webinar with expert Bryan Prince. Learn about air handling and facility design for pharmacy safety.

Facility and Engineering Control Design Under USP 800 White Paper

Facility and Engineering Control Design Under USP 800

Design considerations for creating a Pharmacy USP 800 compliant Hazardous Drug (HD) compounding operation.

Design Tomorrow's Drug Compounding Cleanroom Today

Design Tomorrow's Drug Compounding Cleanroom Today

This white paper covers design considerations to keep in mind when designing your drug compounding cleanroom for the future.

Can a Class I and Class II BSC be in the same Sterile HD Room?

USP 800 does not directly address the pre-sterilization process of a sterile preparation creating the question can a class I and a Class II biosafety cabinet be used in the same sterile HD room?

Budgeting for USP 800

Budgeting for USP 800

Budget considerations for cleanroom construction. Weigh the options between new construction versus remodeling, and other dilemmas that hospital pharmacies may face preparing for USP 800 compliance.