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Non-In Vitro Diagnostic Device Regulatory Submission Table of Contents (nIVD ToC)

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Non-In Vitro Diagnostic Device Regulatory Submission Table of Contents (nIVD ToC)

Please use the comments template to provide comments on the Proposed Document and send comments to Patrick Axtell and Daniel Yoon via email: patrick.axtell [at] fda.hhs.gov (patrick[dot]axtell[at]fda[dot]hhs[dot]gov)  and daniel.yoon [at] hc-sc.gc.ca (daniel[dot]yoon[at]hc-sc[dot]gc[dot]ca)  with the subject line 'Public Consultation on nIVD Table of Contents Working draft’.

Comments Table Template - IMDRF N9 (nIVD ToC) RPS WG