In this rapidly changing environment, your choice of CDMO partner is
critical. The right partnership can serve as your key to commercial success, while the
wrong one can lead to costly delays, quality issues and compliance risks. To help you
overcome your OSD challenges and drug product manufacturing challenges and
streamline your journey to commercialization, our experts have developed an eBook to
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The FDA opened an expedited IND pilot, tightened scrutiny of foreign trial data, and finalized a rule recognizing non-animal testing methods. In Europe, the EMA advanced pharmaceutical legislation reform, restricted 2 legacy products, and opened an injectable-iron safety review.
Ron Scarboro, Azurity Pharmaceuticals, explains why real-world usability belongs at product definition and how post-launch feedback should guide drug formulation.
Gene manufacturing platforms, patient-centric formulations, contract services, packaging innovations, and sterile filling lines are in the spotlight at CPHI Milan 2026.