Drug Discovery & Development Modalities

ChemPartner partners with biotech and pharma across two integrated pillars — Small Molecules (discovery, DMPK & safety, full CMC, and new chemical modalities) and Biologics & Advanced Biologics (antibodies, ADC/RDC, bispecifics, peptides, RNA, gene and cell therapy). One partner. Two decades of sponsor-grade delivery. 2,000+ scientists. A flexible engagement model built around your pipeline.

Experience and scale to move programs forward

For more than two decades, ChemPartner has combined scientific depth, integrated capabilities, and global scale to help partners advance discovery and development programs with confidence. 

Discovery & development
20+ yrs
Scientists worldwide
2,000+
Drugs advanced to clinic
50+
GMP biologics capacity
13,900 L+

Two pillars, one partner

Pillar 01
小分子

From AI-driven design to commercial API and finished dosage form — discovery chemistry, DMPK and safety, full CMC, and new chemical modalities under one project team.

Pillar 02
生物制品与先进生物制品

From DNA to BLA-ready commercial supply — antibodies and the most demanding advanced modalities, integrated across discovery, engineering, and CDMO manufacturing.

小分子

From AI-driven design to commercial API and finished dosage form — discovery chemistry, DMPK and safety, full CMC, and new chemical modalities under one project team.

生物制品与先进生物制品

From DNA to BLA-ready commercial supply — antibodies and the most demanding advanced modalities, integrated across discovery, engineering, and CDMO manufacturing.

Frequently asked questions

How are ChemPartner's modalities organized?

Across two pillars. Small Molecules covers discovery chemistry, DMPK/safety/biology, full CMC (API and formulation, process development to commercial supply), and new chemical modalities (PROTAC, protein degraders, molecular glue). Biologics & Advanced Biologics covers monoclonal antibodies, ADC/RDC, bispecifics, peptides and PDCs, RNA therapeutics, gene therapy, and cell therapies.

Yes — API R&D and manufacturing, formulation development, solid-state R&D, analytical development, process development, pilot scale-up and tech transfer, commercial manufacturing, and a full QMS, supporting IND, 505(b)(2), ANDA, and NDA pathways with IND-enabling packages in as little as ten months.

Yes. Medicinal chemistry, biologics, biology, in vivo pharmacology, DMPK, and toxicology under one project team — ideal for combination strategies such as ADCs, BsADCs, AOCs, PDCs, and degrader-conjugates.

FTE, FFS, blended teams, and risk-share / milestone-based partnerships, with flexibility to scale teams up or down.

Six major sites — Shanghai Zhangjiang (HQ), Shanghai Jinqiao, Shanghai Lingang (API pilot), Jiangsu Qidong (biologics CDMO), Sichuan Chengdu, and Boston — plus offices in Copenhagen, the UK, and partners worldwide.

Royalty-free proprietary libraries, strict project-team firewalls, bilingual SOPs, and a QMS compliant with cGMP, ICH, NMPA, FDA, and EMA.

Ready to advance your next modality?

Whether you’re optimizing a small molecule lead, building a CMC package toward IND, designing a next-generation ADC, or characterizing a cell therapy candidate, ChemPartner’s integrated platform is built to move with you.

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