For medical devices to be subject to clinical investigations, the manufacturer must comply with the provisions of Title II of Book I of Part I of this Code.
For medical devices to be subject to clinical investigations, the manufacturer must comply with the provisions of Title II of Book I of Part I of this Code.
Pour les dispositifs médicaux devant faire l’objet des investigations cliniques, le fabricant se conforme aux dispositions du titre II du livre Ier de la première partie du présent code.
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75001, Paris France
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