DOVER, DE, UNITED STATES, January 21, 2026 /EINPresswire.com/ — The global pharmaceutical supply chain is currently confronting a dual imperative: ensuring ...
In this webinar, attendees will be provided an overview of the technologies that currently exist for bacterial endotoxins testing (BET), and the drawbacks associated with each. Microfluidic technology ...
DOVER, DE, UNITED STATES, June 9, 2026 /EINPresswire.com/ — The safety and quality control of parenteral pharmaceuticals, biologics, and medical devices depend ...
Endotoxin Testing Services from Charles River Labs show up as racks of clear glass vials under cool LED strips, each tiny sample waiting for a robotic arm to slide it into a reader that looks like a ...
With the FDA’s rule in place, sponsors now have clearer regulatory footing to submit nonclinical data generated through validated alternative methods as part of IND and marketing applications, though ...
—New Capabilities and State-of-the-Art Equipment at Irvine Facility Accelerates Turnaround Time and Enhances Quality Control for Sterile Compounds— In response to the increasing demand for fast and ...
As thoroughly covered in your recent article (C&EN, Oct. 28, 2024, page 26), the issue of replacing the traditional natural product test for endotoxin, limulus amoebocyte lysate (LAL), with a ...
The presence of harmful bacteria in parenteral drugs or implantable devices can cause inflammatory responses such as fever and, in some cases, may even be fatal. As a result, robust bacterial ...
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