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process validation

Magellan's validation services division focuses on providing GMP compliance and validation of your facilities, utilities, equipment, products, and processes.

Utilizing our analytical and microbiological strengths, Magellan offers a full range of testing capabilities as well as Master Plan Preparation and Protocol Design/Execution. Our dedicated validation resources offer the technical expertise, pharmaceutical experience, responsive turnaround, and personal commitment to address your needs.

Magellan Pharmaceutical Development can help accelerate your efforts by providing immediate resourcing and technical expertise to make your project a success.

Please give us a call with any questions or submit a project to us online .

Process Validation Services

  • Master Plan Preparation
    • Document Preparation
    • SOPs
    • Protocols
    • Test Methods
  • Cleaning Validation
    • Method Development
    • Protocol Design and Preparation
    • Recovery Testing & Swab Selection
    • Sampling
    • Analytical Testing
    • Microbiological Testing
    • Data Interpretation And Report Preparation
  • Process Validation
    • Project Management
    • Test Protocol Design and Preparation
    • Equipment Qualification
    • Analytical Testing
    • Microbiological Testing
    • Data Interpretation And Report Preparation
  • Capabilities
    • Facilities-Clean Rooms, Isolators
    • Utilities-Air, Water, Gases
    • Equipment-Process related Equipment (Presses, Granulators, Mixers, Sterilizers, Ovens, Fillers)
    • Products-all Dosage Forms (Solids, Parenterals, Liquids, Topicals)
    • Processes-Formulations, Filling, Blending, Packaging, Clinical to Full Scale Production, Sterilization, Aseptic Filling
    • Full Analytical Support
    • Full Microbiological Support
    • Consultation

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