Compare CDMOs manufacturing pharmaceutical cartridges for pen injector devices. Filter by cartridge format, filling capacity, and device assembly experience.
17 companies listed
Pharmaceutical cartridges (1.5mL and 3mL standard formats) are filled with injectable drug product and inserted into reusable or disposable pen injector devices. This dosage form dominates in diabetes (insulin, GLP-1 agonists), growth hormone, and other multi-dose self-administered products. Manufacturing requires aseptic cartridge filling, crimp sealing, and integration with specific pen device platforms.
The GLP-1 agonist boom has created acute demand for cartridge filling capacity. CDMOs with 3mL cartridge filling lines and pen device assembly capabilities are experiencing unprecedented demand. New capacity takes 2-3 years to build and validate, so early engagement with cartridge-capable CDMOs is essential for sponsors developing injectable metabolic disease products.
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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