As an experienced CDMO, our capabilities enable us to successfully partner with pharmaceutical and biotech companies in developing medicines from molecule development to commercialization.

Our teams of scientists have a broad range of chemistry expertise as well as specialized skills which enable us to support our clients throughout the development and manufacturing journey.

Our regulatory-compliant facilities and equipment further enable us to be flexible, efficient, and cost-effective. Our dedicated state-of-the-art laboratories are equipped with automated jacketed reactors (100-5000 mL) can generate 100-200 grams of the final product with desired critical quality attributes (CQAs). We have manufacturing capacity for API scale-up, ranging from 50-150 kg and non-GMP to cGMP production units equipped with 60 kg bulk production of semi-synthetic products.

Chemistry and Reactions
Chemistry and Reactions
Supply Chain Management
Supply Chain Management
Quality Control & Assurance
Quality Control & Assurance
Project Management
Project Management
Regulatory CMC Services
Regulatory CMC Services
Intellectual Property
Intellectual Property
Generic APIs

Generic APIs

More about our service as a dedicated 100% API provider to over 500 customers globally.
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CDMO services

CDMO Services

We are experts in the custom development and manufacturing of new chemical entity (NCE) APIs for pharmaceutical and biotech companies.
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Analytical Development & validation

Analytical Development & Validation

Learn more about our considerable expertise in the development and validation of analytical methods.
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