Auditor GCP
GCP Audit. Part C. GCP Audit course. Data Fabrication and Falsification. Access granted on May 04,2020
GCP Audit. Part C. GCP Audit course. Data Fabrication and Falsification. Access granted on May 04,2020
Auditor GCP
Director, GCP
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 Read more…
Auditor GCP
Senior Clinical Research Associate
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 Read more…
Auditor GCP
Auditor, GCP
Auditor, 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 (QA) to ensure that Read more…
