
Pharmaceutics International, Inc.
Drug product CDMO built for complexity—from potent compounds to commercial scale.
Drug product CDMO specializing in aseptic injectables, oral solid dose, lyophilization, and prefilled syringes with 30+ years of experience in complex formulations and potent compounds; now part of Jabil. Headquartered in Hunt Valley, United States.
Modalities
Development & manufacturing
Structured CDMO capabilities from verified public sources.
Development (D)
Manufacturing (M)
Synthetic chemistry infrastructure
- Capabilities
- HPAPIDEA licensed
Fill-finish formats
Regulatory clearances
Services
- CMC Analytical Development
- Stability Testing & Storage
- Quality Control Testing
- Formulation Development
- Technology Transfer
- Prefilled Syringe (PFS) Filling
- Vial Filling
- Lyophilization (Freeze Drying)
- Sterile Fill-Finish & Aseptic Manufacturing
- Oral Solid Dosage Manufacturing
- HPAPI Manufacturing (High-Potency)
- Secondary Packaging & Labeling
- Serialization & Track-and-Trace
- Process Development
- Controlled Substance Manufacturing
About this organization
Overview
Pharmaceutics International, Inc. (Pii) is a contract development and manufacturing organization (CDMO) specializing in drug product development and manufacturing across early-stage, clinical, and commercial volumes. Acquired by Jabil Inc. on February 3, 2025, Pii combines 30+ years of pharmaceutical manufacturing expertise with Jabil's industry-leading automation and manufacturing capabilities.
Core Capabilities
Formulation & Development Services
- Formulation development focused on bioavailability, stability, and adherence
- Contract analytical services for fast, reliable testing and quality compliance
- Solid-state characterization and complex formulation problem-solving
Manufacturing Services
- Aseptic/Injectables: Sterile fill-finish manufacturing for injectable drug products
- Oral Solid Dose: Custom solutions for tablets, soft gels, and liquid oral formulations
- Lyophilization: Freeze-drying capabilities for injectable products
- Prefilled Syringes: Recent $3.6M investment (November 2024) in advanced labeling, fill/finish, and automated visual inspection technologies
- Controlled Substances: DEA-compliant manufacturing and storage for potent and controlled-substance drugs
Secondary Services
- Packaging, labeling, serialization, and kitting
- Quality assurance and regulatory compliance support
- Technology transfer and scale-up from pilot to commercial production
Facilities & Infrastructure
Four dedicated manufacturing and support facilities in Hunt Valley, Maryland:
- Beaver Court (80,000 sq ft): Aseptic manufacturing and oral solid dose production with DEA vaults
- Gilroy Road (72,000 sq ft): Oral research, development, and manufacturing with DEA vaults
- Beaver Dam (52,500 sq ft): Analytical and quality control laboratories
- Golden West (72,500 sq ft): Labeling, serialization, and kitting operations
Quality & Regulatory
- 100% FDA license to operate
- 300+ scientists and support staff
- 5 drug product approvals in 2023
- 90% of clients report effective solutions delivery
- Emphasis on quality assurance, compliance, and transparency
Certifications
Locations
Beaver Court
Hunt Valley · Maryland · United States
Gilroy Road
Hunt Valley · Maryland · United States
Beaver Dam
Hunt Valley · Maryland · United States
Golden West
Hunt Valley · Maryland · United States
Beaver Court (Aseptic & Oral Dose)
Hunt Valley · Maryland · United States
Gilroy Road (Oral Development & Manufacturing)
Hunt Valley · Maryland · United States
Beaver Dam (Analytical & QC Labs)
Hunt Valley · Maryland · United States
Golden West (Labeling & Serialization)
Hunt Valley · Maryland · United States
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