Place des compléments alimentaires chez les rameurs
Presence of Banned Drugs in Dietary Supplements Following, FDA Recalls
The US Food and Drug Administration (FDA) initiates class I drug recalls when products have the reasonable possibility of causing serious adverse health consequences or death. Recently, the FDA has used class I drug recalls in an effort to remove dietary supplements adulterated with pharmaceutical ingredients from US markets. Approximately half of all FDA class I drug recalls since 2004 have involved dietary supplements adulterated with banned pharmaceutical ingredients.
US Food and Drug Administration Study
JAMA October 22/29, 2014 Volume 312, Number 16.
Authors : Pieter A. Cohen, Gregory Maller, Renan DeSouza, James Neal-Kababick
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Santé et Performance
Notre Société savante a pour mission de promouvoir la Nutrition du sport, dans un objectif de protection de la santé, de recherche de performance, et de prévention des conduites addictives.
Nous proposons des colloques et des journées de formation, fondés sur une actualisation des connaissances scientifiques...
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