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U.S. FDA FCE and SID Requirements

U.S. FDA CITATION: 21 C.F.R. § 108 Subpart B (2015), 21 C.F.R. § 113 (2015), & 21 C.F.R. § 114 (2015)

Registrar Corp FCE-SID experts provide multi-lingual compliance support for FCE facilities, including:

  • Assistance with the FCE registration process, including accessing FDA’s online LACF system
  • Guidance as to required elements, formats, and particularities of FCE-SID submissions
  • FCE-SID Certificates issued by Registrar Corp documenting your valid SID listings to assure your customers that your products have been properly filed with U.S. FDA

Simply complete the form below for assistance with FDA FCE registration and process filing requirements.

  • (include corporate designation such as: Ltd., SARL, S.A., etc.)
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