https://wiki.tiffa.net/w/index.php?action=history&feed=atom&title=Translations%3AVitamin%2F58%2FenTranslations:Vitamin/58/en - Revision history2026-07-10T02:41:42ZRevision history for this page on the wikiMediaWiki 1.43.0https://wiki.tiffa.net/w/index.php?title=Translations:Vitamin/58/en&diff=109589&oldid=prevFuzzyBot: Importing a new version from external source2024-01-19T07:19:09Z<p>Importing a new version from external source</p>
<p><b>New page</b></p><div>===Governmental regulation===<br />
Most countries place dietary supplements in a special category under the general umbrella of ''foods'', not drugs. As a result, the manufacturer, and not the government, has the responsibility of ensuring that its dietary supplement products are safe before they are marketed. Regulation of supplements varies widely by country. In the [[United States]], a dietary supplement is defined under the [[Dietary Supplement Health and Education Act]] of 1994. There is no FDA approval process for dietary supplements, and no requirement that manufacturers prove the safety or efficacy of supplements introduced before 1994. The [[Food and Drug Administration]] must rely on its Adverse Event Reporting System to monitor adverse events that occur with supplements.</div>FuzzyBot