The management of clinical data, from its collection during a trial to its extraction for analysis, has become a critical element in the steps to prepare a regulatory submission and to obtain approval to market a treatment. Groundbreaking on its initial publication nearly fourteen years ago, and evolving with the field in each iteration since then, the third edition of <strong>Practical Guide to Clinical Data Management</strong> includes important updates to all chapters to reflect the current industry approach to using electronic data capture (EDC) for most studies.<br /><br />See what's new in the Third Edition:<br /><br /><br /><br />A chapter on the clinical trial process that explains the high level flow of a clinical trial from creation of the protocol through the study lock and provides the context for the clinical data management activities that follow Reorganized content reflects an industry trend that divides training and standard operating procedures for clinical data manage
0コメント