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Standard classification for tissue engineered medical products(TEMPs)

  • Jung Won So
  • , Soon Hee Kim
  • , Mi Ock Baek
  • , Hye Won Roh
  • , Na Ri Lee
  • , Gyu Ha Ryu
  • , Yang Ha Cho
  • , Seung Jin Lee
  • , Gilson Khang
  • Jeonbuk National University
  • Food and Drug Administration of Korea
  • Ewha Womans University

Research output: Contribution to journal › Journal article › peer-review

Abstract

Tissue engineered medical products (TEMPs) are those protocols and products developed for use in the human body as biological substitutes to restore, maintain, or improve tissue function. So TEMPs may achieve a therapeutic potential from cells, biomolecules, scaffolds, and other materials, and processed tissue and derivatives used in various combinations or alone. Since interactions may occur among the components used in TEMPs, new standard descriptions, test methods, and practices are needed to aid the evaluation of these interactions. Therefore this technical report the aspects of tissue engineered medical that will be developed as standards.

Original languageEnglish
Pages (from-to)124-131
Number of pages8
JournalTissue Engineering and Regenerative Medicine
Volume5
Issue number1
StatePublished - 2008.03

Keywords

  • Biomaterials
  • Cell
  • Classification
  • Standardization
  • TEMPS

Quacquarelli Symonds(QS) Subject Topics

  • Medicine
  • Biological Sciences

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