Title: What Does the Designated Person(s) Do? Speakers: Date: June 24, 2025, 12 p.m. CST Session Description: This presentation will outline the roles and responsibilities
Title: Board of Pharmacy Perspective on Enforcing USP Standards Speaker: Krystal Stefanyk, Director of Inspections, North Carolina Board of Pharmacy Date: March 26, 2025, 12
CONTAMINATION CONTROL: QUALITY CONTROL, LAB TESTING SERVICES Analytical testing refers to the systematic process of evaluating pharmaceutical products, raw materials, or compounded preparations to ensure
Sterility testing of compounded sterile preparations is crucial to prevent patient harm from microbial contamination. USP 797 requires sterility testing for:• Category 2 CSPs which
COMPOUNDING: market leaders usp 797 and 800 Sterile pharmacy compounding refers to the preparation of customized medications in a controlled environment that meets stringent sterility requirements
Get sterility test results in as little as four hours with rapid test methods. Company Background ARL Bio Pharma is a contract laboratory that provides
Media fill testing is a crucial part of personnel qualification and environmental monitoring. During a media fill, technicians use microbiological growth media instead of a
The Pharmacy500 is awarded to 500 supply chain businesses and associations that have made a significant impact on dispensing pharmacies in the U.S. over the
Kathy Heatherly, MSFS, ARL Associate Chemistry Supervisor A bulk substance, or active pharmaceutical ingredient (API), is often the starting point of a compounded preparation. Compounding
Sterility and Endotoxin Kayla Lipcaman, ARL Bio Pharma Associate Microbiology Supervisor Two critical tests for sterile compounded preparations are Sterility and Endotoxin testing. USP 797
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