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 compliance is critical for maintaining safe and reliable standards, but the extensive requirements are demanding.
Download this application note from Sartorius to explore tools and principles for streamlining cGLP and cGMP compliance for liquid handling in pharma quality control.
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The liquid world of fetal development provides a rich source of nutrition and protection tailored to meet the needs of the growing fetus.
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In this webinar, scientists will discuss innovations that are unlocking new insights into immunity.
In this webinar, Magdalena Pacewicz will highlight how to use AUC to characterize AAVs as part of ensuring regulatory compliance.
In this webinar, Andre Mueller will discuss how scientists characterize therapeutic proteins in different formulations and spot the effects of excipients on protein stability.
A streamlined, automated process helps scientists coordinate site-ready production-level whole genome sequencing results.
System strengthens Taiwan’s capabilities in protein drug discovery research
The Transferpette® pro expands the Transferpette® family, offering scientists even greater flexibility to match their pipetting preferences and workflow requirements.
Fast, gentle, and highly specific glycoprotein labeling compatible with downstream immunofluorescence, enabled by next-generation aminooxy chemistry.
Thermo Scientific X and S Series General Purpose Centrifuges are designed to help provide exceptional performance, versatility and enhanced sustainability.
