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  • Services
    • Analytical Services
      • Analytical MD/MV
      • Container – API Compatibility
      • Drug-device Compatibility
      • Extractables and Leachables Testing
      • Forced Degradation and Stability
      • Microbiological Testing
    • Development and Formulation of Sterile Dosage Forms
    • Parenteral & Lyophilized Clinical Trial Materials
    • Commercial Manufacturing – Parenteral & Lyophilized
  • Regulatory
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Analytical Development

By Delaney Wascherol|2020-05-28T08:14:59-04:00May 28th, 2020|0 Comments

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  • Different Types of Viral Vectors for Gene Delivery and How They Are Used
  • What Can We Learn from Non-Touch Techniques for Aseptic Manufacturing?
  • Parenteral Contract Manufacturers Design Efficient Processes to Ensure Compliant Products
  • Necessary Considerations for Viral Vector Development and Manufacturing
  • Syringe Filling at Scale to Deliver on the Increased Demand for Parenteral Product in Pre-Filled Syringes

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    Recent Posts

    • Different Types of Viral Vectors for Gene Delivery and How They Are Used
    • What Can We Learn from Non-Touch Techniques for Aseptic Manufacturing?
    • Parenteral Contract Manufacturers Design Efficient Processes to Ensure Compliant Products
    • Necessary Considerations for Viral Vector Development and Manufacturing
    • Syringe Filling at Scale to Deliver on the Increased Demand for Parenteral Product in Pre-Filled Syringes
    • Aseptic Processing of Sterile Drug Products—Current Industry Best Practices

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    • Parenteral & Lyophilized Clinical Trial Materials
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    5225 Exploration Drive
    Indianapolis, IN 46241

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