AST’s ASEPTiCell® has a unique blend of automated capabilities to ensure your sterile products, whether clinical or commercial, are processed in strict accordance with cGMP requirements. The system has the flexibility to adapt to your process requirements and container options alike, and its ability to process all ready-to-fill vial, syringe, and cartridge formats allow you to bring drug products to market cost-effectively.
By integrating standard process modules into an advanced robotic fill/finish system, the ASEPTiCell provides unrivaled flexibility for cGMP aseptic production of Ready-To-Use Vials, Syringes, and Cartridges, making the ASEPTiCell the ideal fill/finish system for small to medium batch size commercial drug product applications.
The ASEPTiCell can be configured with advanced system features and capabilities to tailor the equipment for each unique application. The system meets the highest standards for aseptic processing by providing features such as environmental monitoring, multiple product dispense system options, in-process fill weight control, and electronic batch record reporting.
Small & Medium Batch Capabilities
The ASEPTiCell is easily configured to process all ready-to-use, nested, vial, syringe and cartridge formats for small and medium commercial batches. The use of highly reliable robotics enables a complete system changeover in as little as thirty minutes. The system can include automated lyo loading and unloading.
Vial Filling, Closing, and Sealing
Syringe Filling and Closing
Cartridge Filling and Closing
Lyo or Lyophilizer Integration
Flexible & Modular System Design
In order to meet a wide range of customer and application needs, the ASEPTiCell has a modular design that provides our customers a system that is tailored to their application requirements without the cost and risk associated with customization. Available modules include:
Semi-Automatic (SABO) or Automatic (ABO) Bag Opening
Automatic Tub Opening (ATO)
Automatic Filling & Closing (FCM)
Lyo Prep (LPM)
Vial Sealing (VSM)
Aseptic Barrier Technologies
ASEPTiCell is integrated with isolator-barrier technologies to fully enclose and tightly control the aseptic environment for ideal conditions for processing sterile drug products. The system can be configured with a Restricted Access Barrier System (RABS) or an aseptic isolator to provide uninterrupted aseptic conditions during production. With isolator integrated systems, the ASEPTiCell is completely compatible with repeated in-situ bio-decontamination using hydrogen peroxide to further enhance the sterility assurance of the system.
Restricted Access Barrier System (RABS)
Isolator – with in-situ bio-decontamination using hydrogen peroxide (VHP)
Small to medium batch production of commercial and clinical materials
Biologics, proteins and potent products
Filling of toxic and cytotoxic materials
Multi-product aseptic filling facilities
Pilot-scale cGMP manufacturing