With PAT, pharmaceutical manufacturers achieve real-time process control, enhancing drug quality and accelerating the ...

QC laboratories perform a critical role in demonstrating pharmaceutical products are consistently manufactured, safe, potent, and pure. At the same time, the number of tests run by QC laboratories is ...

Gas analysis is a crucial aspect of pharmaceutical quality control, which plays a significant role in ensuring the safety and efficacy of drugs. This article discusses the role of gas analysis in ...

Are you ready to revolutionize quality control and deviation management? Discover how AI can empower your organization with process automation, workflow visibility, real-time reporting, and analytics ...

The evolution of quality assurance systems within pharmaceutical entities has accelerated more than any other area over the past 15 years. During this time, a specialized group focused on traditional ...

Researchers engaged in pharma research and development must adhere to current Good Laboratory Practice (cGLP) and Good Manufacturing Practice (cGMP) standard operating procedures. Such regulatory ...

Regulatory expectations align across WHO, EU, PIC/S, and Health Canada; US 21 CFR 211.186/211.188 define MPCR content and faithful BPCR reproduction. Inspection trends highlight uncontrolled page ...

Alternative methods to the use of animals in pharmaceutical testing are becoming more used and accepted. Laura Lotfi of Charles River breaks down the basics of virtual control groups in drug ...