Sterile pharma solution provider

Linkage Production Line Isolator

Linkage Production Line Isolator

The pharmaceutical production line isolator is a highly enclosed physical barrier system, that is used to completely isolate operators, the external environment, and key process areas (such as filling, packaging, weighing, etc.) during the pharmaceutical production process to protect the safety of personnel and the environment.

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Its core functions include:
Sterility assurance: In the production of sterile preparations (such as injections and biological products), maintain a Class A clean environment to prevent microbial contamination.
Cross-contamination prevention and control: In the production of APIs or highly active drugs (such as cytotoxic drugs and hormones), avoid the leakage of harmful substances and protect personnel and environmental safety.
Process stability: Reduce human intervention and reduce the impact of environmental fluctuations on product quality.

Performance and features

  1. Comprehensive product portfolio:isolation systems for water injection, powder injection, prefilled syringe and sterile powder production lines;
  2. Stable and reliable environment:reliable and stable class A environment, which meets cGMP, FDA, ISO, ISPE, and pharmacopoeia requirements;
  3. New VHPS technology:the latest H2O2 sterilization system, which can achieve rapid sterilization, control the concentration and saturation of H2O2, with good sterilization reproducibility;
  4. Intelligent control system:Siemens PLC+IPC control system; intelligent alarms of pressure, H2O2 solution concentration, temperature and humidity, air speed and other monitoring parameters; the system has multi-level access control; comply with FDA 21 CFR part 11 requirements;
  5. Independent temperature and humidity control mode:with the integrated independent air conditioning system, it can realize that the internal temperature and humidity in the chamber is not affected by the external environment;
  6. MOCK-UP:complete wood model verification service, ergonomic operation qualification and 3D model display service in the middle of the project.
  7. Sterilization process development support: qualification and validation services for sterilization cycle development of the whole process can be provided;
  8. Customization:support customized isolation system design, and provide systematic closed isolation solutions and CE certification services;
  9. Integrated monitoring system: integrated monitoring systems of temperature and humidity, differential pressure, air speed, H2O2concentration, optical grating, particles and airborne viable bacteria, etc.;
  10. Multiple sterile transfer solutions:multiple and combined sterile transfer solutions are available to meet customers’ diversified production needs;
  11. Complete life cycle support:covering consulting, project design, installation scheme design and verification design, etc.;
  12. Wireless glove leakage detector: multi-head wired glove leakage detector or wireless glove leakage detector is optional;
  13. CDCV service:sterilization cycle development, validation studies and services;