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Nitto Denko Avecia (NDA) is a contract manufacturer of active pharmaceutical ingredients (API’s) for the pharmaceutical industry. NDA operates under a high-level cGMP quality program supplying material for all clinical phases of development through to commercial scale from FDA inspected facilities in Cincinnati, OH. Services include: manufacture of oligonucleotide medicines (DNA, RNA, siRNA, LNA, and conjugated oligonucleotides), manufacture of small molecule API’s, radiolabeling of oligonucleotides and small molecules, process validation, analytical method development and validation, stability studies, supply chain management, regulatory support, and project management. Nitto Denko Avecia possesses an IP portfolio that permits freedom-to-operate for the manufacture of oligonucleotide medicines.