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FDA Offers Clarity of UDI Application to Kits

By Jodi Scott & Lina Kontos on February 9, 2016
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shutterstock_181648958 (2)On January 4, 2016, FDA officially released a draft guidance document Unique Device Identification: Convenience Kits, with further information regarding the Unique Device Identifier (UDI) requirements for labeling and data submission for kits.

Read More: FDA Offers Clarity of UDI Application to Kits

  • Posted in:
    Health Care and Life Sciences
  • Blog:
    Focus on Regulation
  • Organization:
    Hogan Lovells
  • Article: View Original Source

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