Agenda
2:00 PM — 3:30 PM
WELCOME TO MY WORLD – A DAY IN THE LIFE OF CLINICAL FORUM PROFESSIONALS2:00 PM — 5:30 PM
Workshop 1: THE CLINICAL TRIALS TRANSFORMATION INITIATIVE2:00 PM — 5:30 PM
Workshop 1: THE CLINICAL TRIALS TRANSFORMATION INITIATIVE2:00 PM — 5:30 PM
Workshop 2: ELECTRONIC ARCHIVES ARE NOT YOUR SYSTEM BACKUP MEDIA9:00 AM — 10:30 AM
IMPLICATIONS OF THE NEW PHARMACOVIGILANCE LEGISLATION9:00 AM — 10:30 AM
NEW TECHNOLOGIES TO REBOOT CLINICAL TRIALS - PART I9:00 AM — 10:30 AM
POST-APPROVAL STUDIES AND VIRTUAL STUDIES9:00 AM — 10:30 AM
TRANSLATING DATA INTO INSIGHTS9:00 AM — 10:30 AM
TRANSPARENCY FROM CLINICAL TRIALS11:00 AM — 12:30 PM
MAXIMISING THE VALUE OF POST-APPROVAL STUDIES THROUGH PUBLICATION EXCELLENCE11:00 AM — 12:30 PM
NEW TECHNOLOGIES TO REBOOT CLINICAL TRIALS - PART II11:00 AM — 12:30 PM
PATIENT RECRUITMENT AND RETENTION IN CLINICAL TRIALS11:00 AM — 12:30 PM
PROVE YOUR VALUE! MARKETING MEDICAL INFORMATION11:00 AM — 12:30 PM
RISK MANAGEMENT PLANS4:00 PM — 5:30 PM
CLINICAL DATA STANDARDS: YOUR QUALITY ENABLER4:00 PM — 5:30 PM
CLINICAL TRIAL REGISTRIES4:00 PM — 5:30 PM
IMPROVING CLINICAL DEVELOPMENT PERFORMANCE4:00 PM — 5:30 PM
MI QUALITY4:00 PM — 5:30 PM
PHARMACOVIGILANCE – INNOVATION AND INTERFACES9:00 AM — 10:30 AM
EMERGING MARKETS9:00 AM — 10:30 AM
REGIONAL CONSIDERATIONS9:00 AM — 10:30 AM
RISK-BASED MONITORING – PART I11:00 AM — 12:30 PM
REGIONAL AND GLOBAL MANAGEMENT ASPECTS11:00 AM — 12:30 PM
RISK-BASED MONITORING – PART II11:00 AM — 12:30 PM
STORYLINE DOCUMENTS2:00 PM — 3:30 PM
PATIENT-CENTERED STUDIES - INNOVATIVE APPROACHES TO INCLUDE PATIENTS2:00 PM — 3:30 PM
SUBMISSION CHALLENGES2:00 PM — 3:30 PM
TECHNOLOGY AND SOCIAL MEDIA2:00 PM — 3:30 PM
THE SMART APPROACH TO ePRO4:00 PM — 5:30 PM
BENEFITS OF THE CLOUD4:00 PM — 5:30 PM
HEALTH ECONOMICS OUTCOME RESEARCH (HEOR)4:00 PM — 5:30 PM
SUCCESSFUL REVIEWS4:00 PM — 5:30 PM
THEORY INTO PRACTICEHave an account?