11.05.26 -- Building A Flexible Vaccine Manufacturing Facility With Tonix Pharmaceuticals' Siobhan Fogarty

Optimize containment in oral GLP-1 solid dose manufacturing. Learn how closed single-use containment and flexible isolators secure blending, spray drying, and tableting workflows.

Multi-product ATMP facilities need integrated teams, flexible design, and strategic HVAC to ensure scalability, contamination control, cost efficiency, and reliable long-term performance.

Explore the advantages of 2000 and 3000 L single-use mixing systems and experimental results demonstrating their capacity to deliver high power at large scales and flexibility for use at lower volumes.

Advanced therapies require strict contamination control. See how nuclease-free manufacturing, validation, and testing support quality, compliance, and reliable scale-up.

As manufacturing becomes more flexible and decentralized, sterile connection choices matter more than ever. Examine how portable and fixed tube welders compare and how each supports sterility.

Safeguarding drug quality requires robust stability testing, yet legacy systems often hinder compliance. Discover how modern digital workflows eliminate manual errors and streamline study management.

CLDN6-targeting CAR T cells for solid tumors move from binder discovery through manufacturing, with attention to how process design shapes technology transfer and consistency.

Stay ahead of FDA QMSR, EU GMP, and AI regulations by adopting continuous audit readiness, ALCOA++ data integrity, and closed-loop workflows for global compliance.

Pharma manufacturing embraces cutting-edge automation, yet outdated paper-based documentation hinders efficiency. Take a look at how digital solutions can transform compliance.

Moving from benchtop success to broader use requires scalability. Laboratory automation can reduce variability, improve control, and create a more efficient path toward commercial-ready solutions.

Paper-heavy production can slow decisions and limit flexibility. Find out how IT/OT integration connects shop-floor and enterprise data to support real-time visibility and more resilient operations.

Effective process monitoring relies on selecting the right variables, setting meaningful baselines, and applying consistent analysis. A continuous CPV approach enables earlier detection of variability.

Observe how an integrated, platform-driven CMC approach can accelerate your antibody program from DNA to IND in as little as six months while reducing risk and maintaining quality and regulatory alignment.

Personalized therapies and advanced technologies are reshaping manufacturing. Delve into how intelligent automation can improve flexibility, strengthen data integrity, and accelerate production.