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Lianhe Aigen delivers cutting-edge chemistry-driven innovation across drug discovery, process development, contract manufacturing, and full CMC compliance — accelerating your path from concept to commercialization.
Employees
Scientists
Years of Experience
Lianhe Aigen Pharma Co., Ltd. is a leading provider of innovative drug solutions at home and abroad. Our Shanghai R&D center, Lianhe Aigen Pharmatech Co., Ltd., operates as a CRO platform delivering preclinical new drug discovery services to global clients. Our Taizhou site, formerly known as Lianhe Chemical Technology (Taizhou) Co., Ltd., functions as a fully integrated CDMO platform supporting end-to-end pharmaceutical development and manufacturing.
With a proven track record of compliance and quality, our facilities have been inspected and approved by six key global health authorities including NMPA, FDA, EMA, PMDA, TGA, and KFDA — ensuring reliable, on-time, high-quality delivery for our partners worldwide.
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We offer comprehensive, integrated CRDMO services designed to support pharmaceutical innovation from early discovery through commercial supply.
Full-range chemistry services covering all phases of drug discovery, delivering high-quality compounds from milligrams to kilograms.
QbD-driven process development with expertise in handling complex and hazardous chemicals to deliver robust, efficient, and green synthetic routes.
GMP-compliant manufacturing with facilities approved by FDA, EMA, NMPA, and other global regulators for clinical and commercial supply.
End-to-end CMC solutions including route scouting, impurity control, method development, stability studies, and global regulatory submissions.
Our advanced technology platforms integrate innovation, engineering, and analytical excellence to solve complex challenges in pharmaceutical development.
Technology-driven innovation combining synthesis, analysis, and engineering to deliver novel solutions.
Green chemistry principles with flow chemistry, enzyme catalysis, electrochemistry, and photochemistry in commercial production.
Integrated quality control services including method development, validation, impurity analysis, and stability studies.
Continuous flow processing for safer, scalable, and more efficient synthesis of complex molecules.
Polymorph screening, salt selection, and solid-form optimization for improved drug performance.
Expertise in peptide synthesis, purification, and characterization for therapeutic development.
Design and synthesis of advanced linkers for targeted protein degradation and antibody-drug conjugates.
Full-service support for oligonucleotide synthesis, modification, and analytical characterization.
Our portfolio includes a wide range of high-purity chemical compounds, APIs, and intermediates developed through advanced synthetic technologies.
High-purity peptide building blocks for therapeutic development.
Peptide
Stable, cleavable linkers for antibody-drug conjugate applications.
ADC
Phosphorothioate and 2'-O-methyl modified sequences.
Oligonucleotide
Complex nitrogen-containing scaffolds for kinase inhibitors.
API Intermediate
Asymmetric synthesis with >99% ee for CNS and metabolic targets.
Chiral
Bifunctional molecules for targeted protein degradation.
PROTAC
Beta- and gamma-amino acids for peptide engineering.
Amino Acid
Scalable, safe production of high-energy intermediates.
Flow ChemistryFor business inquiries, product information, or partnership opportunities, please reach out through our official channels.
Lianhe Aigen Pharma Co., Ltd.
No.3 Donghai 8th Avenue, Toumengang New District, Linhai, Taizhou City, Zhejiang Province, China, P.C.317016
Tel: +86 576 8558 1608
Email: [email protected]
Business: [email protected], [email protected]
Careers: [email protected]
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