Ministerio de Salud

Dirección General de Medicamentos, Insumos y Di 01;

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DECENIO DE LAS PERSONAS CON DISCAPACIDAD EN EL PERÚ "Año de la Promoción de la Industria Responsable y del Compromiso Climático"

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Que de acuerdo al Acta de Auditoria de Buenas Prácticas para Laboratorios de Control de Calidad de Productos Farmacéuticos N° 004-1-2014, se concluye que el mencionado laboratorio cumple con las Buenas Prácticas de

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DECENIO DE LAS PERSONAS CON DISCAPACIDAD EN EL PERÚ 'Año de la Promoción de la Industria Responsable y del Compromiso Climático" Ministerio

de Salud NreccIón General

de Medicamentos, in sum y Di lag

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Aplicado a Productos Farmacéuticos No Betalactámicos No Estériles: Area de Sólidos (tabletas con y sin cubierta, tabletas vaginales, cápsulas), Líquidos (jarabes, suspensiones y soluciones). - -

1:411GISSMNICIla,

En base a la Ley N° 29459 Ley de los Productos Farmacéuticos, Dispositivos Médicos y Productos Sanitarios, D.S. N° 014-2011-SA Reglamento de Establecimientos Farmacéuticos y el Anexo 1 del Informe 44° de la Serie de Informes Técnicos de la OMS, N° 957-2010.

Se expide el presente Certificado a solicitud de MEDROCK CORPORATION S.A.C., con razón social LABORATORIOS MEDROCK CORPORATION S.A.C., según expediente N° 14-001061-1 de fecha

V 0015:1 07.01.2014 y Anexo 1 de fecha 05.03.2014• --El.il•-f»,..!-9.410 . .„.. ...... , ,

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