Responsabilità Il CRA/CRC è responsabile del monitoraggio o del controllo di tutte le attività soggette a, “Buona pratica clinica: Linee guida consolidate,” (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 Leggi tutto…
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: Linee guida consolidate,” (GCP/GLP’s), Supportare un programma di garanzia della qualità (QA) to ensure that Allergan project data and summary statements are of known and documented Leggi tutto…
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 Leggi tutto…