https://wiki.tiffa.net/w/index.php?action=history&feed=atom&title=Translations%3AVitamin%2F59%2FenTranslations:Vitamin/59/en - Revision history2026-08-15T04:51:29ZRevision history for this page on the wikiMediaWiki 1.43.0https://wiki.tiffa.net/w/index.php?title=Translations:Vitamin/59/en&diff=109590&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>In 2007, the US [[Code of Federal Regulations]] (CFR) Title 21, part III took effect, regulating Good Manufacturing Practices (GMPs) in the manufacturing, packaging, labeling, or holding operations for dietary supplements. Even though product registration is not required, these regulations mandate production and quality control standards (including testing for identity, purity and adulterations) for dietary supplements. In the European Union, the [[Food Supplements Directive]] requires that only those supplements that have been proven safe can be sold without a prescription. For most vitamins, [[pharmacopoeia|pharmacopoeial standards]] have been established. In the United States, the [[United States Pharmacopeia]] (USP) sets standards for the most commonly used vitamins and preparations thereof. Likewise, monographs of the [[European Pharmacopoeia]] (Ph.Eur.) regulate aspects of identity and purity for vitamins on the European market.</div>FuzzyBot