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Industrial Technology Research Institute

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High-Efficiency Cell Sheet Integration System

Technology Overview

ITRI's cell sheets can be produced directly in the surgical room, streamlining the production process and minimizing the risk of contamination during transportation.
ITRI's cell sheets can be produced directly in the surgical room, streamlining the production process and minimizing the risk of contamination during transportation.

Cell sheets have been a cornerstone of cell therapy for over a decade. ITRI's High-Efficiency Cell Sheet Integration System utilizes a range of biomedical materials, including highly biocompatible substrates, thermal-sensitive biomaterials, specialized aseptic packaging, and customized machine designs. By integrating these technologies, cell sheets can be produced directly in the surgical room, streamlining the production process and minimizing the risk of contamination during transportation.

  • Features
    • Forming temperature control range: 25-50 ℃
    • Cell sheet size: 4 cm×4 cm
    • Cell sheet production rate: one cell sheet can be produced in 30 minutes
    • Printing operation method: operation with one-button touch
  • Specifications
    • Cell sheet can be produced in surgical room
    • Thermal-sensitive biomaterial
    • Simple and convenient man-machine interface
    • Cell sheet is formed in aseptic packaging with no risk of contamination

Applications & Benefits

  • Cell therapy for regenerative medicine
  • Skin tissue repair
  • Tendon injury repair
  • Myocardial tissue damage

Contact

One-Stop Biomedical Services


One-Stop Biomedical Services

  • Listing Regulations Consulting: FDA/TFDA/CE application, medical device verification/export, medical device/medicine registration, IRB document organization, clinical trial application, and more.
  • Technology Transfer: Bio-IT, diagnostics and precision medicine technology, regeneration medicine technology, natural medicine and healthcare technology, targeted drug and delivery technology.
  • Model Translation: Domestic supply chain linkage, medical device design control, market analysis, strategy analysis of regulation in commercialization, and more.
  • Preclinical/Clinical Trial: Functional safety assessments, clinical research organization linkage, clinical evaluation and analysis, clinical trial planning, clinical trial analysis and reports.
  • Other Services: Quality system consulting, commercialization consulting, smart health solutions, software validation, medical device risk management, information security risk evaluation, technical documents preparation, business ecosystem linkage, and more.