GCP Audit. Part C. GCP Audit course. Data Fabrication and Falsification. Access granted on May 08,2023
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…
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…
GCP Auditor certification. Stage 2. Part C. Access granted on May 08,2023 Questions? +447778936902 (WhatsApp) e-mail: head_office@nbscience.com
