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 اقرأ المزيد
GCP Audit. Part C. دورة تدقيق GCP. Data Fabrication and Falsification. Access granted on May 08,2023
مدقق حسابات, GCP Responsibilities The GCP Auditor is responsible for quality assurance auditing of all activities subject to the, “ICH Good Clinical Practice: Consolidated Guideline,” (GCPs), supporting a program of quality assurance (ضمان الجودة) to ensure that AGN project data and summary statements are of known and documented quality. Summary of Responsibilities: اقرأ المزيد
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: Consolidated Guideline,” (GCP/GLP’s), supporting a program of quality assurance (ضمان الجودة) to ensure that Allergan project data and summary statements are of known and documented اقرأ المزيد