Responsibilities The Director, GCP sera tenu de tout superviser et de participer à, audit d’assurance qualité de toutes les activités soumises à la, « ICH Bonnes pratiques cliniques/de laboratoire: Ligne directrice consolidée, » (BPC/BPL’s), soutenir un programme d’assurance qualité (Assurance qualité) 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
Responsibilities The CRA/CRC is responsible for the monitoring or auditing of all activities subject to the, « ICH Good Clinical Practice: Ligne directrice consolidée, » (GCP), 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