A historical partner page describes Stemirna's mRNA vaccine and nanolipid/polymer delivery R&D. The company's website was inaccessible during this review; current operations and clinical status remain unverified.
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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.
471 matching companiesShowing 24 / 471
Yunxin Zhili is a Hangzhou-based service provider supporting process development, manufacturing, and CMC activities for advanced therapies. Its official materials describe plasmid and mRNA services spanning sequence and template preparation, RNA production, purification, LNP formulation, and testing, with targeted LNP development also listed. Manufacturing grade, project scale, timelines, and regulatory suitability require project-specific confirmation.
Levostar Biotech, based in Suzhou, supports nucleic acid and cell and gene therapy projects with plasmid services, RNA synthesis and delivery development, and analytical testing. Its mRNA offering includes sequence design, template construction, RNA production, and LNP formulation. The targeted LNP platform describes antibody conjugation and particle characterization. Manufacturing grade and suitability for a clinical regulatory submission must be confirmed for each project.
Crystal Bio Solutions offers Biologics mass spectrometry, CMC analytics, PK, immunogenicity and biomarkers. Services should be matched to the intended study and assay requirements.
ProtaGene offers Protein structure, impurities, potency and analytical comparability. Services should be matched to the intended study and assay requirements.
BioAgilytix offers Large-molecule PK, ADA, neutralizing antibodies, biomarkers and CMC analytics. Services should be matched to the intended study and assay requirements.
Combines formulation development, clinical pharmacology, and manufacturing, including selection of solubility enhancement technologies, pediatric palatability improvement, and formulation development for multiple administration routes.
Connects spray-dried ASD and particle engineering with oral drug products, offering blending, dry granulation, tableting, coating, and encapsulation from formulation assessment through clinical batches.
Offers drug product CDMO services from formulation design and clinical materials through commercial manufacturing and packaging, including complex oral solids, injectables, and ophthalmic products.
A technology-focused CDMO specializing in small-molecule oral dosage forms, with disclosed formulation and analytical development for taste masking, tailored release, pediatric, and patient-friendly products.
Offers oral, nasal, pulmonary, and early-stage sterile formulation development, from feasibility and prototypes through scale-up and clinical manufacturing, addressing low solubility and stability challenges.
SGS offers Protein characterization, potency, GMP release, stability and bioanalysis. Services should be matched to the intended study and assay requirements.
The unified Bend Bioscience brand brings together the former CoreRx, Societal, and Bend businesses, offering oral solids, oral liquids, ASD, and development from preformulation through process scale-up.
Offers formulation development across a U.S., U.K., and Indian network, with publicly listed nanosuspension, microemulsion, ASD, oral solid, and sterile injectable capabilities.
The development business supports early formulation through registration-batch scale-up and regulatory submissions. Injectable development at Leiden and other sites connects with the group's manufacturing network.
Discloses development from preformulation through final formulation and analytical methods, with expanded bioavailability enhancement for poorly soluble drugs and clinical trial support.
The group has both proprietary drug and CDMO businesses. Publicly disclosed CDMO services cover development and manufacturing of complex oral solids, liquids, semisolids, biologics, and sterile injectables.
Biologics formulation and optimization services include computational analysis, excipient screening, stability, packaging, and high-concentration and in-use studies. The CDMO business is part of the FUJIFILM group.
CMIC's drug product CDMO services cover preformulation, process and analytical development, clinical materials, and commercial supply. Official materials identify CMIC CDMO as part of the Dai Nippon Printing group.
Offers clinical and commercial contract manufacturing for oral solids and injectables, and describes CMC development spanning process and formulation design, analytical work, and regulatory submissions.
The group website lists TPD as a CRO service. Custom offerings explicitly cover target engagement, modulation, and degradation, plus custom proteins, cell lines, and assay development.
Oral dosage development combines spray-dried ASD, HME, particle size reduction, lipid formulations, and controlled release, spanning preclinical and clinical supply through commercial scale-up.
LTS completed its acquisition of the former Renaissance Lakewood business in November 2025 and integrated it into the Nasal & Sterile Drug Products division, offering nasal spray and sterile dosage form R&D and manufacturing.
Canadian contract development and manufacturing services include formulation development, comprehensive physicochemical characterization, development of simple and complex sterile formulations, and aseptic fill-finish.
Coverage expands from sourced records; this database does not claim all biopharma companies.