Régimen transitorio . Los establecimientos que fabriquen, almacenen y/o acondicionen los productos y reactivos de diagnóstico in vitro, tendrán un plazo de veinticuatro (24) meses contados a partir de la fecha de vigencia del presente decreto para gestionar la obtención de los respectivos registros sanitarios.
Decreto 3770 de 2004 →In force
Article 55
Régimen Transitorio
Decreto 3770 de 2004 · por el cual se reglamentan el régimen de registros sanitarios y la vigilancia sanitaria de los reactivos de diagnóstico in vitro para exámenes de especímenes de origen humano.
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