Compare CDMOs manufacturing lyophilized drug products for biologics, peptides, and injectable pharmaceuticals. Filter by dryer capacity, cycle development expertise, and scale.
128 companies listed
Lyophilized (freeze-dried) products are manufactured by removing water from a drug formulation through sublimation, producing a stable dry cake that is reconstituted before use. This dosage form is essential for biologics, peptides, and other molecules that are unstable in liquid form. The lyophilization process occurs after aseptic vial filling, making it an integrated part of the sterile manufacturing process.
Key CDMO selection criteria for lyophilized products include: cycle development expertise (thermal analysis, process optimization), dryer capacity (shelf area determines batch size), scale-up capability (lab to commercial dryers), and integrated fill-finish services. CDMOs offering end-to-end fill-lyophilize-inspect services eliminate the logistics complexity of shipping partially stoppered vials between facilities.
Netherlands
Intravacc is a Netherlands-based vaccine CDMO founded in 2013 with ~200 employees, specializing in vaccine development from discovery through Phase II clinical trials. The company provides cGMP manufacturing of bacterial, viral, conjugate, and oncological vaccines using mammalian and microbial fermentation systems (up to 200L single-use bioreactors), along with comprehensive analytical services and proprietary vaccine platforms including Outer Membrane Vesicle (OMV) technology.
Japan
JCR Pharmaceuticals is a Japanese pharmaceutical company and CDMO founded in 1975, with nearly 50 years of experience in rare disease treatments and orphan drug production. Selected for Japan's Regenerative Medicine CDMO Subsidy Program in 2025, the company is expanding biomanufacturing infrastructure for cell, gene, and regenerative medicine therapies. JCR operates five production sites and has proprietary platforms including JUST-AAV for gene therapy and J-Brain Cargo for blood-brain barrier penetration.
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