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Oligo CDMO

Comprehensive Solution for Oligo Manufacturing

Our goal is to help our customers achieve high quality, scale, and cost-effectiveness through innovation.

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A Comprehensive Solution Provider

Our platform provides a comprehensive solution for oligonucleotide API manufacturing, from preclinical to commercial stages. We have leading capabilities in analytical development, manufacturing, and quality control throughout the entire development process.

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Process Development

Our expertise in development and scaling encompasses a wide range of therapeutic oligonucleotide modifications, such as ASO, siRNA, Aptamer, Oligo conjugates, PMO, and PPMO molecules.  We are continuously researching new technologies to enhance quality and decrease costs. 

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Analytical development

We collaborate with customers throughout the drug development process, method development and transfer, validation, and ICH stability studies to assist in CMC documentation for regulatory filings. We have a wide range of analytical instruments for analyzing oligonucleotides, including raw materials, intermediates, adjuvants, and APIs.


Drug Substance Manufacturing

We have the world-leading capacity for oligo synthesis and downstream processing, supporting API production of batches ranging from a few mmols up to 1800 mmol, at small to commercial-scale. 

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Quality Control

Our QC lab is equipped with advanced equipment to ensure the highest quality control. Our team tests raw materials, intermediates, crude active pharmaceutical ingredients (APIs), and final drug products.