A diversified pharmaceutical platform combining API intermediates, CDMO, drug products, outsourced research and manufacturing, and proprietary product lines.
Company database
Profiles, sources, and comparisons are open. Choose a field on the left to see its companies.
Search & refine Filters update automatically
Disease tags identify mentions in recorded facts or pipeline text, not approved indications or a complete pipeline. Platform service providers may have no disease-specific tag.
473 matching companiesShowing 241–264 / 473
Allucent describes clinical pharmacology strategy, PK/PD, pharmacometrics, modeling, and simulation. Nuventra is part of Allucent and is not counted here as a separate independent provider.
Altasciences offers LC-MS/MS, ligand-binding assays, immunogenicity and biomarkers. Services should be matched to the intended study and assay requirements.
ChemPartner Pharmatech provides discovery, CMC, preclinical, and related research services through operating entities including Shanghai ChemPartner.
ICON lists population PK, PK/PD, exposure-response modeling, trial simulation, first-in-human dose prediction, and formulation-related IVIVC. These are service disclosures, not independent evidence of success for an individual project.
Aanastra discloses PEP-CAR, an anti-CD19 in vivo CAR-T strategy combining engineered RNA and targeting peptides for cancer and autoimmune disease. The public website does not establish a registered clinical program or validated patient outcomes.
Provides ADC and other bioconjugate discovery, process development, and GMP manufacturing, including antibody intermediates and payload-linker capabilities.
Combines products and services across tool compounds, biochemical reagents, molecular building blocks, and API/intermediate/drug-product research and manufacturing.
Extends molecular building-block products into medicinal chemistry, process development, and GMP API/drug-product manufacturing, including continuous-flow technology.
Provides one-stop drug development, regulatory submissions, and CMC/process services, based on clinical and preclinical research capabilities.
Pharmaceutical research subsidiaries provide discovery, CMC, clinical trials, BE/PK bioanalysis, SMO, and marketing authorization holder-related services.
Provides outsourced drug development, clinical, and CMC services, with CDMO and technology commercialization through subsidiaries including Saimer Pharmaceuticals.
AAVivo lists CD19 AVO-100, BCMA AVO-101, and dual BCMA/CD19 AVO-102 using T-cell-targeted AAV. The disclosed activities include vector production and construct optimization, not verified clinical dosing. AVO-103 is a TCR program and is kept separate from CAR-T.
AERA-109 is a targeted-LNP in vivo CAR-T candidate for B-cell-mediated autoimmune diseases, supported by mouse and nonhuman-primate studies. The pipeline projects clinical entry in the second half of 2026; a projected date is not proof that dosing has begun.
Focuses on clinical trial site management (SMO), providing coordination and project execution for sponsors and clinical sites.
Provides CMC, clinical operations, SMO, biosample analysis, data management/statistics, technology commercialization, and collaborative development.
Operates in medicinal and synthetic chemistry, DMPK, process development, and commercial manufacturing, alongside proprietary generic drug research, production, and sales.
Alaya is a preclinical in vivo CAR-T developer. Its disclosed polymeric nanoparticle platform encapsulates lentiviral CAR vectors for targeted T-cell transduction; this is a hybrid polymer/viral approach, not simply a nonviral polymer delivery system.
Combines gene-edited animal-model products and preclinical services with RenMice antibody discovery, licensing/transfers, and collaborative development.
The annual report discloses peptide drug CDMO, generic peptide APIs, and drug products; group financials include proprietary products.
The annual report discloses peptide APIs, self-selected products, and small-molecule CDMO services; this is not a pure-play service company.
The annual report’s key audit matters identify CDMO service revenue of RMB 1.03299 billion; the group also includes heparin APIs and drug products. A/H shares represent one group and are counted once.
The annual report separately discloses RMB 391.9 million in CDMO API/intermediate revenue, alongside generic APIs and drug products.
The annual report confirms CRO services through a virus-assessment platform, including clinical strain testing and antiviral drug/vaccine evaluation for pharmaceutical clients. Drugs and APIs remain the group’s core business; included as diversified.
Coverage expands from sourced records; this database does not claim all biopharma companies.