01.14.26 -- What 2025 FDA Warning Letters Tell Us About GMP Compliance

Know the differences between designing a viral clearance study for non-enveloped viral vectors versus those for mAbs or recombinant proteins, and learn how to identify and remove viral contaminants.

Modern lab equipment is essential to scientific research, but maintaining it is increasingly complex. Discover key challenges and strategies to futureproof your maintenance approach.

This guide ranks fluorochromes, offers pairing strategies, and provides practical tips for designing high-quality, multiparameter assays with clear population separation in your flow cytometry panels.

Read how integrated PCR-based workflows provide the specificity and speed necessary to safeguard your cell matrix and ensure regulatory compliance.

Improve your cleanroom strategy for 2026. Gain actionable insights on leveraging Environmental Monitoring data, optimizing personnel, and managing residue to enhance contamination control.

Learn more about the key features of a high-quality recombinant trypsin and how it can benefit your bioprocess with insightful answers to these common questions.

Explore various innovative qPCR tools that automate and optimize laboratory workflows, and expedite bioanalysis and quality control in the rapidly growing field of cell and gene therapy.