
Greater collaboration and understanding are needed to ensure the correct grade of excipient is used in drug products.

Greater collaboration and understanding are needed to ensure the correct grade of excipient is used in drug products.

In this paper, the authors introduce a method that combines ion exchange chromatography with an easier-to-perform, simpler one-step post-column derivatization that is selective to nitrite and visible spectrophotometric detection to allow high sample loading volumes without affecting resolution.

Insights into molecular behaviors and predictive capabilities are bringing numerous benefits.

New technologies improve efficiency and remove operator intervention.

Viral vectors and other complex biologic modalities require more specificity and higher sensitivity to detect and distinguish contaminants.

Qualifying material suppliers is a crucial step in ensuring safe and effective drug products.

A coordinated and international response is needed to help control the latest mpox outbreak in Africa.

Bio/pharma companies should be approaching their decarbonization journey as a strategic business move for the future as industry stakeholders are placing greater value on sustainability.

Updating your audits and inspections program ensures inspection preparedness, says Siegfried Schmitt, vice president, Technical at Parexel.

What impact will the AI Act have on pharma and digital medicine?

Thermo Scientific’s columns offer fast run times, optimal separation efficiency, and reliable results.

Freudenberg Medical’s new offerings include single-use Y-connector manifolds, tubing assemblies, and bottlecap assemblies, among others.

Charles Ross & Son Company has introduced the ROSS CDA-300 Dual Shaft Mixer, consisting of two agitators and a disperse with an open disc blade.

Asahi Kasei Medical now offers its Planova virus removal filters for use in biopharma manufacturing and plasma derivatives manufacturing.