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FDA GMP 111 Dietary Supplements

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    Grade - AIFSQN

  • IFSQN Associate
  • 41 posts
  • 2 thanks

  • Italy

Posted 05 January 2024 - 08:41 PM

Hi Everyone,


I need your help about the interpretation of the following points about the GMP parte 111 on dietary supplements:


  1. Sec. 111.70 c (1) : does the company has to demonstrate through a validation the in-process specification?
  2. Sec. 111.80: does the company need to collect and hold all the lot code of the dietary ingredients, packaging and label. Do I need to verify each incoming of dietary ingredients?


Thanks you very much for your collaboration in advance,


Best regards


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