07.17.26 -- Cell Therapy Without The Cells: Building A Therapeutic Secretome With Noveome Biotherapeutics' Larry Brown, Sc.D.

Discover how a proactive, risk-based supply chain strategy can help strengthen resilience, mitigate disruption, and ensure continuity across your biotech and pharmaceutical operations.

Explore the differences between liquid nitrogen and mechanical cryogenic freezers, and learn how each method supports scientific, medical, and industrial storage needs.

Unlock high-quality transcriptome data from degraded or low-input samples with a 6.5-hour workflow and enhanced sensitivity for rare transcripts and viral detection, even from FFPE tissues.

Read about how diagnosing ribosome pausing sites and optimizing codon usage dramatically improves bispecific antibody titers, turning difficult-to-express candidates into viable therapeutics.

Gain insights that can support your next steps, whether advancing to a new clinical phase, constructing a new facility, or fine-tuning an existing process to keep pace with market shifts.

Delve into how Organ-on-Chip technology significantly enhances drug development processes and improves the accuracy of clinical translation, leading to more effective and reliable therapeutic outcomes.

Integrated analytics address multispecific antibody CMC challenges, accelerating timelines, reducing risk, and improving decisions through mechanism-driven bioassays, automation, and real-world case studies.

Compress your biologics process characterization timeline without sacrificing quality. Learn how FMEA, DoE, and platform approaches help you hit PPQ readiness faster while managing regulatory risk.

Eliminate regulatory risks caused by fragmented data. Find out how a continuous data thread from bench to batch streamlines tech transfer and accelerates filing timelines.

Cell polarity, the asymmetric organization of eukaryotic cells, is vital for tissue development and homeostasis, but intracellular assembly of the protein complexes involved remains unclear.

High-purity trypsin and carboxypeptidase B enable critical protein processing in manufacturing. See how animal-free, GMP-grade production meets quality standards for growing operations.

Uncover how to implement PAT effectively with a roadmap that covers techniques, validation, data integrity, and lifecycle strategies to help teams improve quality, control, and productivity.

Examine how lyophilization revolutionizes biologic drug manufacturing and ensures potent, stable treatments for complex diseases.