The merger of Kindeva Drug Delivery and Meridian Medical Technologies creates a leading CDMO with robust drug-device capabilities.
The merged organization offers expansive end-to-end services for government and private entities with support from 9 R&D facilities.
The new Kindeva better meets an expansive array of client needs with enhanced development and manufacturing capabilities for life-changing therapies and high-quality products.
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.