Substantial equivalence (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Substantial equivalence" in English language version.

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ask-force.org

biosafety.be

  • Organisation for Economic Co-operation and Development. Report of the Task Force for the Safety of Novel Foods and Feeds C(2000)86/ADD1. May 17, 2000 [1] Archived 2016-03-11 at the Wayback Machine

biotech-info.net

bund.de

bfr.bund.de

  • Schauzu, Marianna (Apr 2000). "The concept of substantial equivalence in safety assessment of foods derived from genetically modified organisms" (PDF). AgBiotechNet. 2.

doi.org

fao.org

fda.gov

  • "Premarket Notification 510(k)". US Food and Drug Administration (FDA). 16 Sep 2015. Retrieved 5 February 2016.
    "A 510(k) is a premarket submission made to FDA to demonstrate that the device to be marketed is at least as safe and effective, that is, substantially equivalent, to a legally marketed device ... that is not subject to PMS [Premarket Approval]. Submitters must compare their device to one or more similar legally marketed devices and make and support their substantial equivalency claims."

harvard.edu

ui.adsabs.harvard.edu

isaaa.org

loc.gov

nih.gov

pubmed.ncbi.nlm.nih.gov

oecd.org

semanticscholar.org

api.semanticscholar.org

web.archive.org

weebly.com

thebeuselaer.weebly.com