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El registro sanitario de productos farmacéuticos es indispensable, debido a que es la vía más efectiva que tienen para poder fabricarse, envasarse e importarse hacia el consumidor final (que en este caso sería la sociedad). Se entiende, pues, como un riguroso proceso por el cual se autoriza a una persona natural o jurídica el poder […]
On December 03, 2020, Idaly Jazminy Morote Guzmán, our Quality Assurance Specialist and Coordinator of Regulatory Affairs for Medicines and Biological Products, participated on behalf of SCR Consultores – Peru Headquarters, in the Technical Meeting: Proposal for Changes in the Regulation of Dietetic Products and Sweeteners – DIGEMID, which […]
On December 11, 2020, Rosa Campos Yaipén, our Specialist in Regulatory Affairs & Coordinator of Pharmacovigilance and Drug Safety, participated on behalf of SCR Consultores based in Peru, in the Workshop III: Challenges of Bioequivalence to exchange Generic Medicines, which was organized and convened by LATFAR. The speakers at this […]
On January 21, 2021, Walther Vicente Mallma, Specialist in Quality Assurance and Coordinator of Regulatory Affairs for Health Products and Medical Devices, and Ronald Quiñonez Dextre, Analyst for Regulatory Affairs and Pharmacovigilance, participated on behalf of SCR Consultores based in Peru. the Technical Meeting “Pharmacovigilance of Vaccines against COVID-19 […]
On January 22, 2021, Ronald Quiñonez Dextre, our Regulatory Affairs and Pharmacovigilance Analyst, participated in the technical meeting on the Technical Document "Manual of Good Pharmacovigilance Practices RM 1053-2020/MINSA", which was convened by the Ministry of Health of Peru, and carried out through the virtual platform Zoom, this […]
On December 09, 2020, Walther Vicente Mallma and Alberto Conislla Vigo, members of our Medical Devices and Health Products Regulatory Affairs team, participated on behalf of SCR Consultores, Peru headquarters, in the Virtual Technical Meeting of the Diagnostic Sector, which was convened by COMSALUD, belonging to the Chamber of […]
On December 04, 2020; Rosa Campos Yaipén, our Pharmacovigilance and Drug Safety Coordinator, participated on behalf of SCR Consultores, based in Peru, in the Workshop II: Good Pharmacovigilance Practices “Implementation Challenges in Latin America”, which was organized and convened by LATFAR. The speakers at this event were Dr. […]
On December 11, 2020, Gianfranco Castro Camacho and Walther Vicente Mallma, members of our Quality Assurance and Regulatory Affairs teams for Medical Devices, participated on behalf of SCR Consultores, Peru headquarters, in the Virtual Workshop: Cold Chain Management in Pharmaceutical Products. and Biological “Challenges and advances in Latin America”, […]
On December 10, 2020, Mary Carmen Chuquimia Socpaza, our Quality Specialist and Regulatory Affairs Coordinator, participated on behalf of SCR Consultores, Bolivia headquarters, in the technical meeting on the Socialization of the Stability Study Guide, which was convened by The State Agency for Medicines and Technologies in […]
On November 27, 2020; Rosa Campos Yaipén and Mary Carmen Chuquimia Socpaza, members of our Pharmacovigilance and Regulatory Affairs teams, participated on behalf of SCR Consultores based in Peru and Bolivia, respectively, in the first technical meeting on Pharmacovigilance, which was convened by the State Agency for Medicines and Technologies in […]