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A Medical Device Clinical Auditor’s Favorite Regulation: 21 CR 812.100

  
  
  
A Medical Device Clinical Auditor%27s Favorite Regulations

I am often asked by industry colleagues that if I had to pick just one “favorite” federal regulation what would it be?  The answer is easily 21 CFR 812.100, as this regulation embodies 95% of the investigational site non-compliances  I observe as I conduct clinical investigator audits. Let me elaborate.

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