Responsibilities The CRA/CRC is responsible for the monitoring or auditing of all activities subject to the, « ICH Good Clinical Practice: Consolidated Guideline, » (GCPs), supporting client programs administrated by Watermark ensure project data and summary statements are of known and documented quality. Requirements Will be expected to travel extensively to study 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 (QA) to ensure that Allergan project data and summary statements are of known and documented Lire la suite
Short List of Commonly Used Acronyms in Clinical Research 700U Statement of Economic Interest ACRP Association of Clinical Research Professionals AE Adverse Event ADR Adverse Drug Reaction AMA American Medical Association BID Twice Daily BIND BiologicalIND CAP Collegeof American Pathologists CBCTN Community Based Clinical Trials Network CBER Centerfor Biologics Evaluation and Lire la suite