
Description
Catalent is a leading global provider of advanced drug development and manufacturing solutions, helping pharmaceutical companies bring better treatments to market.
Catalent partners with pharmaceutical, biotech, and consumer health companies to optimise and accelerate the development, delivery, and supply of medicines, biologics, and health products. With a network of facilities worldwide and expertise in various delivery technologies, Catalent enhances product quality and expands access for patients globally.
Key Products and Services
- Drug Development Services: Preclinical to commercialisation support, including formulation and analytical services.
- Biologics: Advanced cell and gene therapy capabilities, protein therapies, and viral vector manufacturing.
- Drug Delivery Solutions: Expertise in oral, inhalation, injectable, and transdermal delivery technologies.
- Clinical Supply Services: Comprehensive support for clinical trials, including packaging and distribution.
Catalent’s mission to enhance patient care through innovative solutions makes it a trusted partner in the pharmaceutical and biotechnology industries. With state-of-the-art facilities, cutting-edge technologies, and a global reach, Catalent continues to shape the future of healthcare delivery.
Manufacturing Information
Capabilities
- Accelerated Stability Studies
- Aerosol
- Agglomeration
- Analytical Methods Development
- Analytical Services
- Anti-Counterfeiting
- Antibody-Drug Conjugates
- API Solubilization Technologies
- APIs (Active Pharmaceutical Ingredients)
- Asceptic Fill-Finish
- Assay Development
- Auditing
- Banding
- Barcoding
- Bioanalytical Services
- Bioavailability Studies
- Biological Testing
- Biologics
- Biomarker Research
- Bioprocess Validation
- Bioprocessing
- Biosimilars
- Blister
- Capsule
- Cartridge
- Cell and Gene Therapy
- Cell Culture Media Development
- Chemical Analysis
- Chemistry (CMC)
- Chromatography
- Classifying
- Clinical Dose
- Clinical Packaging
- Clinical Trial Materials
- Clinical Trials
- Cold Chain Management
- Cold Form
- Comparator Drugs
- Consulting
- Containment
- Contract Development
- Contract Development and Manufacturing (CDMO)
- Contract Packaging
- Contract Research (CRO)
- Controlled Release
- Controlled Substances
- Creams & Ointments
- Custom Synthesis
- Cytotoxic & High Potency Compounds
- Disposable/Single-Use
- Dissolution Testing
- Distillation
- DMF Establishment / Maintenance
- Dosage Form Development
- Dose Form
- Drug Delivery Devices
- Drug Product Formulation (FDF)
- Encapsulation
- Environmental Analysis
- Feasibility Studies
- Filling
- Fluid Bed Processing
- Formulation Development
- Gels
- Glass
- Granulation
- High Throughput Screening
- Hot Melt Extrusion
- IND/NDA Submissions
- Injectables
- Labelling
- Liquids
- Lot Release Testing
- Lyophilization
- Mammalian Cell Culture
- Mass Spectrometry
- Metabolic Analysis
- Microbiological Testing
- Micronization
- Mixing & Blending
- Nasal Delivery
- Non Sterile Dosage
- Nutraceuticals
- Ophthalmics
- Oral Drug Delivery
- Organic Synthesis
- OTC
- Packaging
- Parenterals
- Particle Size Analysis
- Pharmacogenomics
- Physical Testing
- Pilot-Scale Filling
- Preclinical Testing
- Preformulation
- Process Analytical Technology (PAT)
- Process Development
- Process Validation Studies
- Protein and Peptide
- Protein Extraction/Purification
- Quality Management Systems
- Quality QA/QC
- Regulatory Services
- Research & Development
- Scale-Up
- Screening
- Small Molecule
- Soft Gels
- Solid Dosage
- Solutions & Suspensions
- Spray Drying
- Stability Studies
- Sterile
- Sterile Filling
- Sterility Testing
- Storage
- Supply Chain & Logistics
- Sustained Release
- Sustained Release Delivery Systems
- Syringe
- Tablet Coating
- Tablets
- Technology Transfer
- Testing
- Topicals
- Unit Dosage
- Vaccines
- Validation
- Vials
- Warehousing
Contact Information
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