Description
Curia is a global contract research, development, and manufacturing organisation (CDMO) that partners with pharmaceutical and biotechnology companies to transform ideas into real-world impact.
Founded in 1991 as Albany Molecular Research, Inc. (AMRI), Curia has evolved over three decades to offer a comprehensive suite of solutions across the drug development spectrum. With deep scientific expertise and a robust global network, Curia provides flexible and scalable services to accelerate the delivery of products to patients.
Key products and services include:
- Small Molecules: Offering strategic solutions for early drug discovery services, compound development, and manufacturing.
- Generic Active Pharmaceutical Ingredients (APIs): Providing the capacity to meet clientsr complex products on time.
- Biologics: Delivering comprehensive capabilities from discovery to Good Manufacturing Practuring.
- Sterile Fill-Finish: Specialising in clinical and commercial sterile manufacturing.
- Analytical Services: Offering a complete range of analytical solutions to support discovmercialisation.
With over 30 years of experience, Curia remains a dedicated ally to its clients, navigating thdrug discovery, development, and manufacturing with unwavering commitment and collaboration at its core.
Capabilities
- Accelerated Stability Studies
- ADMET
- Analytical Services
- Animal Health
- Antibody-Drug Conjugates
- API Solubilization Technologies
- APIs (Active Pharmaceutical Ingredients)
- Asceptic Fill-Finish
- Assay Development
- Bioanalytical Services
- Biocatalysis
- Biologics
- Bioprocess Validation
- Bioprocessing
- Biosimilars
- Cartridge
- Cell and Gene Therapy
- Cell Culture Media Development
- Certification
- cGMP Synthesis
- Chemical Analysis
- Chemistry (CMC)
- Chiral Separations
- Chromatography
- Classifying
- Cleaning Equipment
- Clinical
- Clinical Dose
- Clinical Packaging
- Closures
- Combinatorial
- Consulting
- Containment
- Contaminant Analysis
- Contract Development
- Contract Development and Manufacturing (CDMO)
- Contract Packaging
- Contract Research (CRO)
- Controlled Substances
- Custom Synthesis
- Cytotoxic & High Potency Compounds
- Design & Testing
- DMF Establishment / Maintenance
- Dosage Form Development
- Dose Form
- Downstream Processing
- Drug Delivery Devices
- Drug Development
- Drug Screening
- Excipients
- Fermentation
- Filling
- Filtration
- Fine Chemicals
- Formulation Development
- Generics
- Granulation
- High Potency
- High Throughput Screening
- ICH
- IND/NDA Submissions
- Injectables
- Intermediates
- Large Volume
- Lead Optimization
- Library Synthesis
- Lipids/Phospholipids
- Liquids
- Litigation Support & Discovery
- Lyophilization
- Mammalian Cell Culture
- Medicinal
- Metabolic Analysis
- Microbial Fermentation
- Micronization
- Microscopic Analysis
- Mixing & Blending
- Non Sterile Dosage
- Ophthalmics
- OTC
- Packaging
- Parenterals
- Parenterals Development
- Particle Size Analysis
- Pharmacology
- Physical Testing
- Pilot-Scale Filling
- Powders
- Preclinical Testing
- Preformulation
- Process Analytical Technology (PAT)
- Process Characterization
- Process Development
- Process Validation Studies
- Protein and Peptide
- Protein Synthesis
- Purification
- Quality QA/QC
- Raw Materials Analysis
- Regulatory Services
- Research & Development
- RNAi Technology
- Scale-Up
- Screening
- Solid Dosage
- Solid State
- Solutions & Suspensions
- Spray Drying
- Stability Studies
- Sterile
- Sterile Filling
- Sterility Testing
- Sterilization
- Storage
- Syringe
- Technology Transfer
- Testing
- Toxicology Services & Analysis
- Training
- Trays
- Unit Dosage
- Vaccines
- Validation
- Vials
- Wet Chemical Analysis
- X-Ray Crystallography
- X-Ray Powder Diffraction
- X-Ray Spectroscopy