Grand River Aseptic Manufacturing vs Pfizer CentreOne

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Category	Grand River Aseptic Manufacturing	Pfizer CentreOne
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.	Award-winning CDMO specializing in commercial manufacturing of oral solids, sterile injectables, and biologic drug products with Pfizer's technical expertise and global network.
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	Oral Solid Dosage Manufacturing Sterile Fill-Finish & Aseptic Manufacturing Vial Filling Prefilled Syringe (PFS) Filling Cartridge Filling Lyophilization (Freeze Drying) ADC (Antibody-Drug Conjugate) Manufacturing Technology Transfer CMC Analytical Development Process Development Formulation Development Stability Testing & Storage Quality Control Testing CMC Regulatory Submission Support Biologics Development & Manufacturing
Modalities	Small Molecule Biologics (Monoclonal Antibodies) Biologics (Other) Vaccine	Small Molecule Biologics (Monoclonal Antibodies) Biologics (Other) Antibody-Drug Conjugate (ADC)
Indications	Data not yet provided.	Data not yet provided.
Locations	Headquarters, Grand Rapids, Michigan, United States Headquarters	Data not yet provided.
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.