Commercial Sterile Drug Product Locations
Albuquerque, NM, US
Bulk Capacity 1-1200 L
GMP Dose Filling Lines Vials, syringes & cartridges
Validated For 2 – 100 mL vials 1 – 10 mL syringes
Non-cyto Liquid and lyophilized
Cyto/Highly Potent Liquid and lyophilized
Expertise and Capabilities
Microfluidization/high-shear homogenization/extrusion
Suspensions/emulsions/liposomal/nanoparticles
Small molecule
Proteins/peptides/oligonucleotides
Monoclonal antibodies (mAbs)
Inactivated and attenuated live virus
Late phase clinical and commercial
Full in-house QC /Microbiology services (including sterility testing)
Stability Services
Quality and Regulatory
FDA and EU Approved
DEA registration for Schedule II-V controlled substances
Burlington, MA, US
Bulk Capacity 1 – 200 L
GMP Dose Filling Lines Vials and syringes
Validated For 2 – 50 mL vials 1 – 10 mL syringes
Non-cyto Liquid and lyophilized
Cyto/Highly Potent Liquid
Expertise and Capabilities
Process Development
Highly viscous formulations
Microfluidization/high-shear homogenization/extrusion
Suspensions/emulsions/liposomal/nanoparticles
Small molecule
Proteins/peptides/oligonucleotides
Monoclonal antibodies (mAbs)
Clinical and commercial
In-house QC capabilities
Stability Services
Quality and Regulatory
FDA and EU Approved
DEA registration for Schedule II-V controlled substances
The power of a partnership with Curia
Deep expertise
cGMP manufacturing for 50+ commercialized products
Controlled substance capabilities
DEA registration (Schedule II-V)
Various formats
Vials, syringes and cartridges
Continuous improvement
$200 million investment expanding Albuquerque, NM facility
