Grand River Aseptic Manufacturing vs Stevanato Group

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Category	Grand River Aseptic Manufacturing	Stevanato Group
Listed site	cdmo	cdmo
Summary	Sterile injectable CDMO specializing in fill-finish services for liquid and lyophilized vials, syringes, and cartridges, with Annex 1 compliant facilities and experience in biologics, small molecules, and vaccines.	Leading global provider of integrated drug containment, drug delivery, and diagnostic solutions with 75+ years' experience in glass primary packaging, contract manufacturing, and analytical services across development, clinical, and commercial stages.
Services	Sterile Fill-Finish & Aseptic Manufacturing Vial Filling Prefilled Syringe (PFS) Filling Cartridge Filling Lyophilization (Freeze Drying) Quality Control Testing Secondary Packaging & Labeling Serialization & Track-and-Trace Stability Testing & Storage CMC Analytical Development Technology Transfer CMC Regulatory Submission Support Controlled Substance Manufacturing Vaccine Manufacturing Monoclonal Antibody (mAb) Manufacturing Biologics Development & Manufacturing API Synthesis & Manufacturing Small Molecule Development & Manufacturing	Vial Filling Cartridge Filling Prefilled Syringe (PFS) Filling Sterile Fill-Finish & Aseptic Manufacturing Secondary Packaging & Labeling Serialization & Track-and-Trace CMC Analytical Development Stability Testing & Storage Extractables & Leachables Studies Quality Control Testing Combination Product Assembly & Final Packaging Technology Transfer
Modalities	Small Molecule Biologics (Monoclonal Antibodies) Biologics (Other) Vaccine	Biologics (Monoclonal Antibodies) Peptide mRNA Oligonucleotide Antibody-Drug Conjugate (ADC) Vaccine Biologics (Other)
Indications	Data not yet provided.	Metabolic
Locations	Headquarters, Grand Rapids, Michigan, United States Headquarters	Fishers, Fishers, Indiana, United States Monterrey, Monterrey, Mexico Zhangjiagang, Zhangjiagang, China
Certifications	GMP · Identifier: Five GMP manufacturing facilities Annex 1 · Identifier: Three facilities designed and qualified with Annex 1 revisions GMP · Identifier: Five GMP manufacturing facilities; three Annex 1 compliant FDA · Identifier: GMP EMA · Identifier: Annex 1 GMP · Identifier: Five GMP manufacturing facilities (three Annex 1 compliant)	Data not yet provided.
Reviews	Review summary appears after site-level review signal gate opens.	Review summary appears after site-level review signal gate opens.