Auditor, GCP Responsibilities The GCP Auditor is responsible for quality assurance auditing of all activities subject to the, «Buenas prácticas clínicas de la ICH: Guía consolidada,» (GCP), apoyar un programa de garantía de calidad (control de calidad) Garantizar que los datos del proyecto AGN y los resúmenes sean de calidad conocida y documentada.. Resumen de responsabilidades: Leer más
Responsibilities The Director, GCP will be required to oversee all and participate in, quality assurance auditing of all activities subject to the, «ICH Good Clinical/Laboratory Practice: Guía consolidada,» (GCP/GLP’s), apoyar un programa de garantía de calidad (control de calidad) to ensure that Allergan project data and summary statements are of known and documented Leer más
Responsibilities Assisting in the design and execution of high quality clinical studies in compliance with FDA and ICH requirements. Function as a primary liaison to clinical investigators/site staff. Identify, qualify, initiate, monitor and close out clinical sites. Co-monitor with CRO when issues arise with the site. Assist in the selection Leer más
GCP Audit. Part C. Curso de auditoría de GCP. Data Fabrication and Falsification. Access granted on May 08,2023