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FDA Circular 2013-07 Registration of Human Stem Cell-based Products

  • Writer: CCIP Secretariat
    CCIP Secretariat
  • Jul 8, 2013
  • 1 min read

The FDA issued a regulatory framework to ensure access to sae and quality health facilities engaging in human stem cell and cell-based or cellular therapies in the Philippines.

To read the full circular, http://www.cciphilippinesinc.com/uploads/UserFiles/File/update/FC2013-017-%20Registration%20of%20Human%20Stem%20Cell-Based%20Products.pdf

 
 
 

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