USP <797> sets minimum standards for compounded sterile preparations to prevent exposure to particulate matter that may cause patient harm. Particulate matter is the unwanted
Join ARL Bio Pharma in Chapel Hill, NC, for the North Carolina Board of Pharmacy’s Compounding Summit, March 6-8, 2024. NCBOP has great speakers who
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
With supply chain issues, product release schedules, and the timeliness of contamination investigations, the need for a rapid sterility testing solution is greater than ever
Wed, Sep 29, 2021 2:00 PM – 3:00 PM EDT Using quality raw materials in compounding is important to mitigate patient safety risks. This session
What is particulate matter and why is testing performed? Particulate matter is unwanted solid material in solutions for injection. Particle counts that exceed USP limits
Dispense Drugs Faster with Rapid Sterility Advantages of Releasing Drugs from Quarantine Earlier • Decrease costly drug waste • Decrease internal drug shortages • Improve
Dispense Drugs Faster with Rapid Sterility Advantages of Releasing Drugs from Quarantine Earlier • Decrease costly drug waste • Decrease internal drug shortages • Improve
Dispense Drugs Faster with Rapid Sterility Advantages of Releasing Drugs from Quarantine Earlier • Decrease costly drug waste • Decrease internal drug shortages • Improve
