Capability
Packaging & Labeling CDMOs
Compare CDMOs with pharmaceutical packaging and labeling capabilities including blister packaging, bottling, serialization, and clinical trial labeling.
494 companies listed
About Pharmaceutical Packaging & Labeling
Packaging and labeling is the final manufacturing step before distribution. Primary packaging (blisters, bottles, vials, pouches) directly contacts or contains the product. Secondary packaging (cartons, inserts, cases) provides information and protection. Both must comply with regulatory requirements for labeling content, child resistance, and serialization/track-and-trace.
Serialization is now mandatory in most major markets. The Drug Supply Chain Security Act (DSCSA) in the US, EU Falsified Medicines Directive (FMD), and similar regulations globally require unique serial numbers on each unit, enabling track-and-trace through the distribution chain. CDMOs must have validated serialization lines integrated with their packaging operations.
Companies (494)
Biose Industrie
France
Biose Industrie is a French CDMO specialized in microbiome therapeutics, established in 1951. They focus on manufacturing Live Biotherapeutic Products (LBPs) and Next-Generation Probiotics (NGPs) for pharmaceutical and consumer health markets. They combine aerobic and anaerobic microbiology expertise with industrial-scale GMP manufacturing. Investing EUR 80 million to expand capacity from 8,000L to 32,000L fermentation volume at their Aurillac site. They offer full CDMO services from process development to GMP drug product manufacturing.
Biologics Drug SubstanceBiologics Drug ProductFill/Finish (Vials)
BioTechnique LLC
United States
BioTechnique LLC is a full-service CRDMO based in York County, Pennsylvania, specializing in cytotoxic and therapeutic sterile injectable fill-finish services. The company provides services from investigational/clinical through to final marketed products, handling both small and large batch sizes. BioTechnique operates an FDA-registered facility with capabilities spanning sterile manufacturing, lyophilization, and high-potency compound handling.
Frequently Asked Questions
What packaging formats are available at CDMOs?+
Common formats include: blister packaging (PVC, PVC/PVDC, cold-form aluminum), bottle packaging (HDPE, glass), carton packaging, pouch and sachet filling, kitting for clinical trials, and specialized formats (unit-dose, compliance packaging). For sterile products, the primary container (vial, syringe) is typically filled during the fill-finish step, with secondary packaging done separately.
What is clinical trial labeling and packaging?+
Clinical trial packaging involves: labeling per regulatory requirements (blinded or open-label), randomization and kit assembly, temperature-controlled packaging for cold chain products, expiry date management, and distribution logistics to clinical sites. CDMOs offering clinical packaging (sometimes called "clinical supply" services) manage the complexity of multi-country, multi-language, investigational product distribution.
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