Compare CDMOs specializing in biologics drug product formulation, aseptic fill-finish, and packaging for vials, syringes, and autoinjectors.
161 companies listed
Biologics drug product (DP) manufacturing transforms the purified drug substance into the final formulated, filled, and packaged product. This includes formulation optimization (excipient selection, concentration, pH, surfactant), sterile filtration, aseptic filling into primary containers, optional lyophilization, visual inspection, labeling, and secondary packaging.
Protein stability drives formulation complexity. Biologics are susceptible to aggregation, deamidation, oxidation, and fragmentation. The formulation must protect against these degradation pathways throughout the shelf life. CDMOs need scientists experienced in protein characterization and stability-indicating assay development.
Germany
Vetter Pharma is a leading global Contract Development and Manufacturing Organization specializing in aseptic fill-and-finish services for injectable drug products. Headquartered in Ravensburg, Germany, Vetter operates as an independent, family-owned business with over 75 years of experience.
Canada
ResolveMass Laboratories Inc. is a Canadian pharmaceutical CRO and CDMO providing analytical testing, characterization, and drug development support for pharmaceutical, biotechnology, and medical device companies worldwide. Our expertise spans small molecules, peptides, biologics, biosimilars, oligonucleotides, polymers, and complex drug products. We offer specialized services including mass spectrometry (LC-MS/MS, LC-HRMS), peptide characterization, impurity identification, nitrosamine analysis, extractables and leachables (E&L) studies, bioanalytical testing, stability studies, method development, and regulatory support. Our multidisciplinary scientific team helps clients address complex analytical challenges and generate high-quality data to support research, development, manufacturing, and regulatory submissions. ResolveMass Laboratories operates from Canada and serves clients across North America, Europe, and Asia. The company maintains an ISO 9001:2015 certified Quality Management System, is FDA-registered, and holds a Health Canada Drug Establishment Licence for GMP-compliant operations. We are committed to delivering scientifically rigorous, reliable, and timely solutions that accelerate drug development and support regulatory success.
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