
Description
Founded in 1998, CorePharma is a "Quality Driven + People Powered" U.S. based Oral Solid Dosage CDMO with a strong compliance track record. Our focus is on providing our clients with a platform for success. We provide comprehensive end-to-end solution, from development through to commercial launch, back by our industry-leading customer service. Our state-of-the-art development, analytical, manufacturing and packaging facilities uphold the highest quality standards, with a total annual capacity of 5 billion dosage units - covering development, pilot scale and commercial operations. CorePharma continuously invests in cutting-edge technologies and capabilities, ensuring we are the one-stop shop for all your CDMO needs.
Type of Drugs Manufactured:
Small Molecule
CDMO Services:
Research & Development;Packaging;Regulatory Services;Analytical Development
No. of Manufacturing Facilities:
3-5
Facilities Locations:
North America
Regulatory Approvals for facilities:
FDA (United States);ISO;GMP
Manufacturing Technologies:
Liquids;Solids
Company Products and Services:
CMO/CDMO
Current Capacity:
Our facilities currently have available capacity and are ready to take on new client projects. We are well-equipped to handle additional development and manufacturing needs and would be happy to discuss how we can support new business.
Capabilities
- Accelerated Stability Studies
- Analytical Methods Development
- Analytical Services
- Blending
- Blister
- Capsule
- Chemistry (CMC)
- Clinical Trial Materials
- Clinical Trials
- Contract Development and Manufacturing (CDMO)
- Contract Packaging
- Contract Research (CRO)
- Controlled Release
- Controlled Substances
- Dissolution Testing
- Dose Form
- Drug Development
- Drug Product Formulation (FDF)
- Encapsulation
- Filling
- Fluid Bed Processing
- Formulation Development
- Generics
- Granulation
- Labelling
- Liquids
- Mixing & Blending
- Mixing and Granulating Equipment
- Non Sterile Dosage
- Nutraceuticals
- Oral Drug Delivery
- OTC
- Packaging
- Particle Size Analysis
- Photostability
- Pilot-Scale Filling
- Powders
- Preclinical Testing
- Preformulation
- Process Development
- Process Validation Studies
- Project Management
- Quality QA/QC
- Raw Materials Analysis
- Regulatory Services
- Research & Development
- Samples
- Scale-Up
- Serialization
- Small Molecule
- Solid Dosage
- Solutions & Suspensions
- Stability Studies
- Sustained Release
- Tablet Coating
- Tablets
- Technology Transfer
- Unit Dosage
Contact Information
AI and Digital Manufacturing Benchmarking Survey
Take this quick 5 minute assessment to benchmark your organisation’s digital and AI maturity — and see how you compare with industry peers.