cGMP Manufacturing Services

cGMP Manufacturing Services
Product Description

Our Operations team has extensive experience in cGMP clinical drug product manufacturing. Our state-of-the-art facilities and cGMP compliant systems are specifically designed for quick-to-clinic operations. Eurofins CDMO’s team of Engineers, Technology Transfer specialists, and Scientists specialize in process transfer and scale-up strategies, providing a seamless transition of programs from development through cGMP manufacturing.cGMP Manufacturing Services Capabilities:
• High Containment Operations
• cGMP Clinical Manufacturing (Oral Dosage Forms)
• Nanomilling - Wet Milling
• Micronization - Jet Milling
• API-in-Capsule
• Encapsulation and Tableting
• Liquid and Suspensions
• Amorphous Dispersions
• cGMP Stability and Drug Product Release
• cGMP Storage and Distribution

Eurofins CDMO Alphora Inc

  • CA
  • 2015
    On CPHI since
  • 3
    Certificates
Company types
Contract Service
Manufacturer/Innovator

Eurofins CDMO Alphora Inc

  • CA
  • 2015
    On CPHI since
  • 3
    Certificates
Company types
Contract Service
Manufacturer/Innovator

More Products from Eurofins CDMO Alphora Inc (4)

  • Early Phase Support

    Product Early Phase Support

    From the lab to the plant:• Development of new, scalable API route options
    • Process safety and hazards assessment
    • cGMP starting material assessment& establishment of regulatory concept
    • Starting material & other raw materials sourcing and development
    • Polymorph screening & salt...
  • Phase 2 Support

    Product Phase 2 Support

    Setting the stage for the commercial process:• Route or step rebuild
    • Process optimization &demonstration
    • Impurities assessment & synthesis
    • Full structure characterization &elucidation
    • Analytical method development &qualification
    • Stress studies & ICH stability st...
  • Phase 3 or Commercial Support

    Product Phase 3 or Commercial Support

    Taking the molecule to market• Fate & purge studies
    • Impurities marker synthesis &qualification
    • Design of experiments
    • Critical process parameters studies
    • Preparation for, and execution ofprocess validation
    • Continuing CMC support during &after market launch
    • Technolog...
  • API Development Services

    Product API Development Services

    Eurofins CDMO is an FDA-approved contract development and manufacturing organization (CDMO) focused on process chemistry, cGMP scale-up and analytical method development for complex, small molecule APIs, including highly potent molecules. Our talented team of Process Research, Analytical, Technology Transf...

Eurofins CDMO Alphora Inc resources (1)

  • Brochure Analytical Services 2021

    Eurofins CDMO offers analytical services as part of API development as well as stand-alone analytical testing services for projects at various stages in the drug life cycle (pre-clinical to late phase). Our analytical scientists specialize in the development of analytical methods and phase appropriate specifications to ensure control of the synthetic process and quality of API throughout the program.