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Le statut de médicament, au sens de spécialité pharmaceutique, a été attribué réglementairement par la Communauté Européenne (CE) aux produits dérivés du plasma (PDP) par sa directive du 14 juin 1989. Cette directive impose à tous les établissements membres de la CE de respecter la réglementation en vigueur relative aux médicaments pour la préparation, le contrôle et l'enregistrement des PDP. La réglementation...
Set the date range to filter the displayed results. You can set a starting date, ending date or both. You can enter the dates manually or choose them from the calendar.