by Jeffrey Wotton | Oct 31, 2023 | Insights
Ensuring Quality Excellence: Understanding cGMP in Biopharma In the dynamic industry of biotechnology and pharmaceuticals, ensuring the highest standards of quality and safety is paramount. cGMP, or Current Good Manufacturing Practices, should be the fundamental, core...
by Jeffrey Wotton | Oct 23, 2023 | Case Study, Working Reference Standard, Working standard qualification
Creating Working Reference Standard (WRS) Qualification Protocols Approved and ready to use WRS qualification protocols significantly reduce workload, time and resources when transitioning from one WRS lot to another. Primary reference standards (PRS), secondary...
