GCP Audit. Part C. GCP Audit course. Data Fabrication and Falsification. Access granted on May 08,2023
Auditeur, GCP Responsibilities The GCP Auditor is responsible for quality assurance auditing of all activities subject to the, « ICH Good Clinical Practice: Consolidated Guideline, » (GCP), supporting a program of quality assurance (QA) to ensure that Lire la suite
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 Lire la suite
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 Lire la suite