Life sciences manufacturers leading development of new drug and vaccine products realize that new technologies are the strategic drivers of innovation, safety, and speed. Recent events further highlight the criticality of having strong production strategies in place.

Honeywell believes you can efficiently ramp up production of potential medical solutions to full-scale manufacturing automation while still in clinical trials. Parallel path development of automation can start with minimum details of the final formulation. Imagine digitizing the currently manual steps during clinical trials to prepare electronic submittals for regulatory review, and then using that data to prepare final automation design with real-time enterprise-wide visibility and predictive insights.

This webinar illustrates how to:
• Rapidly configure an automation system,
• Seamlessly link with the most modern equipment from any vendor,
• Leverage virtual and cloud solutions, flexible control compute, and lean project implementation,
• Become scalable and flexible to demand fluctuations,
• Go from approval to production in months depending on processing needs.

Learn more about how to serve the needs of patients at an expedited pace.