English 
Español 
Ronald Erik Quiñonez Dextre, Regulatory Affairs and Pharmacovigilance Analyst de nuestra sede SCR Consultores Perú, ha realizado un Análisis Regulatorio sobre «Principales consideraciones para la elaboración de informes periódicos de seguridad de Productos Farmacéuticos en el Perú», el cual les invitamos a revisar en el siguiente enlace: Descargue PDF en Español Download PDf in English
Library Scope of Resolution No. 886: «Guide for Medicine Stability Studies in Bolivia Mary Carmen Chuquimia, Quality Specialist & Regulatory Affairs Coordinator of our headquarters SCR Consultores Bolivia, has carried out a Regulatory Analysis of the recently approved «Guide for Drug Stability Studies in Bolivia» Drug Stability in Bolivia”, which we invite you to review […]
Library Regulatory Aspects for the Reconditioning of Pharmaceutical Products and Medical Devices in Peru Milagros Arista Arévalo, Quality and Regulatory Affairs Specialist at our headquarters SCR Consultores Peru, has carried out the Regulatory Analysis "Regulatory Aspects for the Reconditioning of Pharmaceutical Products and Medical Devices in Peru" , which we invite you to review in the following […]
Library Regulatory Aspects to take into account for the Harmonization of Pharmaceutical Product Labeling in Bolivia and Peru Jazminy Morote Guzman, QA Specialist & Biologics and Drug Regulatory Affairs Coordinator of our headquarters SCR Consultores Peru together with Mary Carmen Chuquimia, Quality Specialist & Regulatory Affairs Coordinator of our headquarters SCR Consultores Bolivia, […]
Library Regulatory Aspects of the Verification and Validation of the Design of Medical Devices SCR Consultores shares the following Regulatory Analysis «Medical Devices: Regulatory Aspects of the Verification and Validation of the Design of Medical Devices», carried out by QF Walther Ricardo Vicente Mallma, who is QA Specialist & Medical Devices and Sanitary Products Regulatory Affairs Coordinator […]
- 1
- 2