Search CDMOs

• CMC Analytical Development
• CMC Regulatory Submission Support
• Combination Product Assembly & Final Packaging

Lifecore is a sterile injectable CDMO with 60 years of regulatory experience, offering end-to-end services including formulation and process development, aseptic manufacturing, fill-finish, analytical testing, stability, and assembly and packaging for drugs, biologics, medical devices, and combination products.

• CMC Analytical Development
• Downstream Processing
• Microbial Fermentation

Germany-based CDMO specializing in GMP-compliant microbial production of recombinant proteins, peptides, plasmid DNA, and bacterial vaccines with bioreactor capacity up to 1,500 litres and regulatory clearance from FDA, EMA, ANVISA, PMDA, and MFDS.

• CMC Analytical Development
• Biologics Development & Manufacturing
• Cell-Line Development

End-to-end CDMO specializing in protein-based biologics and gene therapies, with 20+ years of expertise and cGMP facilities in Lithuania and Massachusetts supporting development from preclinical to commercial stages.

• CMC Analytical Development
• Cartridge Filling
• Sterile Fill-Finish & Aseptic Manufacturing

Argonaut is a sterile fill-finish CDMO specializing in isolator-based aseptic manufacturing for biologics, peptides, nucleic acids, lipid nanoparticles, gene therapies, and vaccines from preclinical through commercial scale, with FDA and Annex 1 compliance.

• CMC Analytical Development
• API Synthesis & Manufacturing
• Process Development

Clearsynth delivers advanced deuterium science, isotopically labelled compounds, custom synthesis, and specialized CDMO services for small-molecule drug discovery and development. ISO 17025, ISO 17034, and ISO 9001:2015 certified with capabilities spanning reference standards, generic APIs, process development, and scale-up manufacturing.

• CMC Analytical Development
• API Synthesis & Manufacturing
• CMC Regulatory Submission Support

Privately held small molecule CDMO with FDA-inspected cGMP facilities in Italy, USA, and China, offering custom manufacturing, development, and specialized technologies including HPAPI, continuous flow, and cryogenic API synthesis from early-stage to commercial scale.

• ADC (Antibody-Drug Conjugate) Manufacturing
• CMC Analytical Development
• API Synthesis & Manufacturing

Porton is a global CDMO offering integrated manufacturing and development services across small molecules, peptides, oligonucleotides, biologics, and conjugates with specialized capabilities in flow chemistry, biocatalysis, and advanced therapies.

• ADC (Antibody-Drug Conjugate) Manufacturing
• CMC Analytical Development
• Cell-Line Development

Oklahoma-based CDMO specializing in antibody-based therapeutics from cell line development through cGMP manufacturing. Offers ModularCMC platform with phase-appropriate work packages and high-touch project management.

• CMC Analytical Development
• CMC Regulatory Submission Support
• Cold-Chain Storage & Logistics

Vancouver-based CDMO delivering technology transfer, formulation development, and GMP manufacturing for 75+ molecules across oncology, diabetes, and respiratory therapeutics since 2005.

• CMC Analytical Development
• Formulation Development
• Oral Solid Dosage Manufacturing

Confab is a recognized CDMO offering contract manufacturing, formulation development, technology transfer, and analytical services for prescription, over-the-counter, generic, controlled, and veterinary pharmaceuticals across liquid, solid, and semi-solid dosage forms.

• ADC (Antibody-Drug Conjugate) Manufacturing
• CMC Analytical Development
• Cell Therapy Manufacturing

UK-based fill-finish CDMO offering rapid access to GMP aseptic manufacturing for clinical and commercial injectable drug products across mAbs, ATMPs, ADCs, RNA, peptides, vaccines, and small molecules.

• CMC Analytical Development
• Cold-Chain Storage & Logistics
• Combination Product Assembly & Final Packaging

Specialist powder-handling CDMO offering clinical trial supply, development, manufacturing, and packaging services for pharmaceutical products.

• CMC Analytical Development
• API Synthesis & Manufacturing
• CMC Regulatory Submission Support

Contract development and manufacturing organization (CDMO) offering complex chemical synthesis, process development, API manufacturing, and supply services for pharmaceutical clients globally.

• CMC Analytical Development
• Combination Product Assembly & Final Packaging
• Sterile Fill-Finish & Aseptic Manufacturing

US-based CDMO specializing in complex life science, in vitro diagnostic, drug-device combination products, lyophilized formulations, and reagent manufacturing with 45 years of industry experience and 200+ life science partners.

• AAV Manufacturing
• CMC Analytical Development
• Cell-Line Development

Full-service CDMO offering cGMP and non-GMP mammalian, microbial, gene therapy, and cell therapy manufacturing from preclinical to commercial scale, with bioreactor capacity up to 50,000L.

• CMC Analytical Development
• Formulation Development
• Lyophilization (Freeze Drying)

USA-based CDMO specializing in lyophilization R&D, formulation development, and small-batch manufacturing for pharma and diagnostics. ISO 13485 and ISO 9001 certified with 35+ years of industry experience.

• CMC Analytical Development
• Formulation Development
• Oral Solid Dosage Manufacturing

Fee-for-service CDMO specializing in formulation development, process development, and GMP manufacturing of oral dosage forms from preclinical through Phase II, with proprietary KinetiSol amorphous solid dispersion technology for poorly soluble APIs.

• CMC Regulatory Submission Support
• Secondary Packaging & Labeling
• Quality Control Testing

Medical device CDMO offering design, engineering development, clinical and commercial manufacturing, plus 60+ years of expertise in desiccant primary packaging for moisture-sensitive pharmaceuticals.