We're proud to receive a 2025 CDMO Leadership Award in the “Small Molecule Dosage Form” global category.
Biotech and biopharma sponsors partnering with Thermo Fisher Scientific through our Accelerator™ Drug Development’s 360° CDMO and CRO solutions gain numerous benefits, including speed, flexibility, and cost savings. From process development to commercial manufacturing, there are opportunities for improvement throughout the drug development journey.
In a recent video, Jennifer Cannon, president of commercial operations, pharma services at Thermo Fisher Scientific, discusses findings from a recent study by the Tufts Center for Drug Development, focusing on oncology. She demonstrates how an integrated CDMO and CRO approach can help reduce clinical drug development timelines by an average of 7-19 months.
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