Title: Prepping Fill/Finish Systems to Ensure Quality Output

A holistic approach to validation and quality assurance is essential. Biologic drugs are highly valuable in treating diseases, and assurance of sterility and proper final product quality is essential. Appropriate testing must be conducted to ensure the filled vials, syringes, cartridges, etc. contain the correct quantity of sterile, contaminant-free product. Aseptic process simulations are crucial for the assessment of aseptic filling capabilities. The main goal …

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   Application Sequencing
 325412 - Pharmaceutical Preparation Manufacturing                
Company  Product  Process  Other  Subjects  Event  Event  Date  Location  Publication  Publication  Date Text  Descriptor
  • Manufacturing Units

  • Handling & Delivery Systems

 

 

 

 

  • BioPharm International

 

  • 12/1/2020

 

  • Article