Pharmaceutical CDMO services
We support consistent quality control from raw materials to active pharmaceutical ingredients, including method development and stability testing!
Otsuka Chemical Co., Ltd. offers pharmaceutical CDMO services. Utilizing organic synthesis technology cultivated over many years in pharmaceutical manufacturing, we provide a consistent service from special raw materials to intermediates and mid-sized active pharmaceutical ingredients. With over 60 years of experience in halogenation technology and our unique catalyst development technology, we respond to diverse needs. Please feel free to contact us when you need our services. 【Features】 ■ High pharmacological activity (OEB Category 4) with solid-phase synthesis / flow synthesis capabilities Newly established GMP-compliant multi-purpose plant ■ Consistent service from special raw materials to intermediates and mid-sized active pharmaceutical ingredients ■ Responding to diverse needs through halogenation technology and unique catalyst development technology *For more details, please refer to the PDF document or feel free to contact us.
basic information
[Nucleic Acid Drug Synthesis Services (Example)] <Lab Synthesis> ■ Basic Framework: Antisense, SiRNA, Aptamer, miRNA, etc. ■ Nucleotides: Natural & Special (Amidite contract synthesis available) ■ Modifications on Phosphate: PO/ PS/ Chimera ■ Specification of Manufacturing Conditions: Available ■ Synthesis Amount (per batch): Several mg to several g *For more details, please refer to the PDF document or feel free to contact us.
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Applications/Examples of results
For more details, please refer to the PDF document or feel free to contact us.
