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Because of the potential for product shortages at pharmacies, the FDA has not only given industry more time for compliance—but time to catch up on boosting the supply chain’s interoperable efforts.
A crash course on the bubble itself, including therapeutic areas most affected.
Addressing the bottlenecks in cell and gene therapy manufacturing through a well-designed artificial intelligence approach is essential to avoiding data siloes.
December 13, 2024
In the fourth part of this roundtable discussion, key opinion leaders discuss how successful RFID use cases in the food sector can translate well to pharma, including what needs to be implemented in order to see success.
Bill Trombetta, PhD, professor, healthcare strategy, marketing, St. Joseph's University, discusses the breakout session at Trade & Channel Strategies in Philadelphia.
A session provides considerations for manufacturers during development, rollouts, and implementation, specifically as it pertains to the HSSP perspective.
December 12, 2024
Kevin O’Meara discusses Patient-Cetric 3.0 breakout session and the challenges of drug manufactures implementing Direct-to-Patient models.
A session investigates the drivers of these shortages and ways to mitigate them.
The latest news for pharma industry insiders.
December 11, 2024
Breakout session explores how direct-to-patient models shorten the time to diagnosis and therapy to improve patient outcomes.
The seminar focuses on US supply chain resiliency, while remaining compliant and preserving patient access.
A case study explores a way to potentially transform commercial organizations, while driving revenue growth.