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Zhejiang Tailin Biotechnology Co., Ltd
Cell preparation workstation
NegotiableUpdate on 02/13
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Overview
The cell preparation workstation is a closed integrated operating system specifically designed for cell product preparation and meets GMP sterile production requirements. It can replace traditional GMP laboratories by integrating functional equipment such as cell separation, activation, modification, amplification, observation, collection, and packaging, and providing a continuous sterile operating environment for cell products.
Product Details
Product Usage
Suitable for the cultivation and production preparation of the vast majority of engineered cell products on the market, applied to large hospitals, cell research institutions, cell therapy companies, etc.
Product Features
1. Provide a Class A clean environment for the entire process of cell production operations, in compliance with GMP sterile requirements.
2. By adopting an integrated vaporized hydrogen peroxide sterilization system, rapid sterilization and transfer of samples can be achieved, and effective biological decontamination can be carried out on the operating area and material channels.
3. Real time recording of system control and environmental monitoring data, as well as recording and storing of operation videos, to achieve data traceability throughout the entire production process.
4. Workstations can be designed modularly and freely combined according to customer needs.
5. Personalized design based on process requirements, integrating various key equipment required for installation process.
6. Compact integrated design effectively saves space without the need for large building layouts.
7. Just need to install on D-levelandaboveIn a clean environment, the construction and operation costs of high-end cleanrooms have been reduced.
Meets professional standards
1. Complies with the requirements of the appendix for Chinese GMP cell therapy products
2. Meet the production requirements of Chinese GMP sterile products
3. Comply with the technical guidelines for research and evaluation of Chinese cell therapy products
4. Meet the requirements of relevant regulations and industry guidelines (ISO, PDA, USP, and Chinese Pharmacopoeia) of various regulatory agencies (FDA, EMA, NMPA)
