Brand New, Unread Copy in Perfect Condition. A+ Customer Service! Summary: Overview of Clinical Research. FDA Regulations and Good Clinical Practice Guidelines. The Study: Planning Stages and Commencement. Interactions with the Sponsor. Interactions Within the Institution; The Role of the Study Subjects. Data Management: Adverse Events. Investigational Agent Management and Inspection of Clinical Research Sites. Codice inventario libreria
Riassunto: This revised edition of a bestseller provides a logical, step-by-step guide to testing new drugs and treatment modalities in compliance with the latest FDA regulations. With current forms, ICH GCP information, FDA regulations, and other references, it shows readers how to manage a clinical research study effectively and efficiently.
Condizione libro: New
Descrizione libro CRC Press, 2001. Ring-bound. Condizione libro: New. 2 Lslf. Codice libro della libreria DADAX1574911236