Articles

Regulatory Sourcebook 2021 

Many details must be considered to maintain a successful disinfection program. These details can make a big difference in a critical environment.

Details Make the Difference for Successful Disinfection v2

This paper explores the most important data challenges experienced by the rapidly modernizing pharmaceutical industry and proposes a GxP-compliant, ready-made application as a solution designed to increase efficiency in upstream processes, while maintaining data integrity and compliance.

Improve Yield and Predict Anomalies in Your Bioreactor

Ask these five questions to find a smart CDMO partner for your projects. Probe strategically to experience fewer manufacturing issues, faster approval, and higher ROI. 

Five “Must Ask” Questions for CDMOs v2

Peak Deconvolution Unlocks the Full Potential of PDA Data

Technical Review of Twin Screw Extrusion Technologies for Life Science Applications v5

Lessons from Industry Roundtable: Regulatory Roadblocks Around Decentralized Trials

This tech note evaluates intra- and inter-system retention time and peak area precision for the analysis of two active pharmaceutical ingredients and their related impurities

All Whitepapers