Webinar Overview: Out of specifications (OOS) are an inevitable part of the pharmaceutical manufacturing environment, and no part of the process is immune from them
No rapid detection solution has ever been put together like this before. Now that we’ve done it, it’s hard to picture it any other way.
No rapid detection solution has ever been put together like this before. Now that we’ve done it, it’s hard to picture it any other way.
How revised chapters of USP regulations impact pharmaceutical production to increase patient safety This December, the United States Pharmacopeia (USP) updates for General Chapters (GC)
Bacterial Endotoxins Test in Biomed Devices and Medications Workshop February 17 and 19th in Centro Coyol Costa Rica, Alajuela Register Here Microbiología Farmacéutica is a
Rapid ATP-Bioluminescence Testing Delivering accurate, reliable compounding sterility results in days rather than weeks. PRIMARY INTENDED OUTCOME Quality control testing is an essential step during
Rapid ATP-Bioluminescence Testing Delivering accurate, reliable compounding sterility results in days rather than weeks. PRIMARY INTENDED OUTCOME Quality control testing is an essential step during
QC Microbial Solutions for Compounding Pharmacies Pharmacies that prepare individualized dosages of sterile, high-risk drugs for patients must meet stringent requirements and standards that protect
