The development and release of pharmaceutical products require the use of modern, efficient, and adaptable analytical techniques to assure efficacy and patient safety. The growing interest in complex ...

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 ...

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 ...

With the publication of ICH Q2(R2) and ICH Q14, the modern Quality by Design (QbD) paradigm introduced by ICH Q8 for manufacturing has now been extended to Quality Control (QC). A life cycle and ...

The study makes clear that regulators expect human oversight to remain central to pharmaceutical quality assurance. Human operators must participate at key control points and retain authority to ...

Analytical quality control refers to all those processes and procedures designed to ensure that the results of laboratory analysis are consistent, comparable, accurate and within specified limits.

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 global Molecular Spectroscopy Market is poised for remarkable growth, projected to nearly double from USD 7.3 billion in ...

In liquid packaging, filling accuracy defines both efficiency and credibility. Even small volume errors can lead to waste, ...

India’s pharmaceutical industry is projected to target a size of $ 130 billion by 2030, more than double its current size of $ 58 billion in 2024. As the "Pharmacy of the World," India holds a unique ...

Round Insights → Stay ahead with quarterly and annual data updates: Across the UK, healthcare facilities and pharmaceutical ...