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DIGEMID INFORMS THAT THE DATA OF THE RESPONSIBLE FOR PHARMACOVIGILANCE AND TECHNOVIGILANCE IN THE COUNTRY SHOULD BE COMMUNICATED

DIGEMID  a través del comunicado publicado el 30 de abril de 2019 en su Portal Institucional, hace de conocimiento  en cumplimiento con  la NTS N° 123-MINSA/DIGEMID: “Norma Técnica de Salud que regula las actividades de Farmacovigilancia y Tecnovigilancia de Productos Farmacéuticos, Dispositivos Médicos y Productos Sanitarios”,  que  los Titulares de Registro Sanitario y del Certificado de Registro Sanitario de los productos farmacéuticos y dispositivos médicos, deberán comunicar los datos del responsable de Farmacovigilancia y Tecnovigilancia en el país.

Source: DIGEMID

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Dictate provisions referring to the requirement of the Certificate of Good Manufacturing Practices for the registration and re-registration in the Sanitary Registry and in the importation of pharmaceutical products

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MODIFY ANNEXES OF VARIOUS RR.MM. REGARDING DIGEMID ADMINISTRATIVE PROCEDURES PROCESSED BY THE VUCE, IN ORDER TO UPDATE THE LIST OF SUCH PROCEDURES

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