Bacterial endotoxin testing is a critical component of quality assurance in sterile compounding and pharmaceutical production. Charles River Laboratories offers Endosafe® cartridge technology, a system
Environmental Monitoring Performance Qualifications (EMPQ) and pharmaceutical water system qualifications are designed to demonstrate sustained microbiological control. While correct organism identification is essential, the real
Asembia’s AXS26 Summit April 26 – 30, 2026 | Las Vegas, NV The exhibit hall in Wynn’s Cristal Ballroom is buzzing with energy, bringing together
Why settle for slow, traditional methods when speed and accuracy are within reach? Celsis® minimizes change and strengthens your regulatory path. Get faster results, greater capacity,
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
Sterile compounding pharmacies, whether small 503A hospital facilities or large 503B GMP-compliantoutsourcing sites, face increasing pressure to meet evolving quality standards while protecting patients from
A lot has happened in the world of sterile, compounded medicine in the past decade – from the creation of sections 503A and 503B in
Our Endosafe(R) cartridge brochure offers in-depth insights into advanced endotoxin testing techniques, providing streamlined, rapid, and precise solutions that are not typically found in traditional
On August 1, 2025, the United States Pharmacopeia (USP) released Chapters <73> and <1071>, simplifying the adoption of ATP-bioluminescence-based Rapid Microbiological Methods (RMMs) like Celsis® for
In the realm of pharmaceutical compounding, ensuring the sterility and safety of preparations is paramount. Charles River offers a comprehensive suite of microbial solutions designed
