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| DEPT | SUBJECT | NUMBER | CREDITS | COURSE NAME | Web Site |
| HCS | NUR | 1800 | 2 (credits) | COORDINATING CLINICAL TRIALS | not available |
| THE PURPOSE OF THIS COURSE IS TO PROVIDE INDIVIDUALS WITH A BASIC UNDERSTANDING OF CLINICAL TRIALS RESEARCH CONDUCTED IN ACCORDANCE WITH FEDERAL REGULATIONS. ASPECTS OF CLINICAL TRIALS RESEARCH SUCH AS REGULATORY REQUIREMENTS, INFORMED CONSENT, PRE AND POST STUDY ACTIVITIES, AUDIT PROCEDURES, AND BUDGETARY ISSUES WILL BE COVERED. THIS COURSE WILL IN CLUDE PRESENTATIONS BY INDIVIDUALS EXPERIENCED IN CONDUCTING TRIALS; CLINICAL RESEARCH COORDINATORS, IRB STAFF, INVESTI GATIONAL PHARMACISTS, STATISTICIANS, AND OTHER EXPERTS IN CLINICAL RESEARCH. | |||||