アジェンダ
8:00 AM — 8:30 AM
8:30 AM — 8:45 AM
8:45 AM — 9:30 AM
SESSION 1: DRUG DEVELOPMENT9:30 AM — 10:15 AM
SESSION 2: QUALITY FRAMEWORK10:15 AM — 10:45 AM
10:45 AM — 11:45 AM
SESSION 3: REGULATORY OVERVIEW11:45 AM — 12:30 PM
SESSION 4: CLINICAL DEVELOPMENT12:30 PM — 1:30 PM
1:30 PM — 2:00 PM
SESSION 5: STUDY DESIGN2:00 PM — 3:30 PM
SESSION 6: STUDY PLANNING3:30 PM — 4:00 PM
4:00 PM — 5:30 PM
SESSION 6 (CONTINUED): STUDY PLANNING5:30 PM — 6:30 PM
8:30 AM — 10:15 AM
SESSION 7: RESOURCING10:15 AM — 10:45 AM
10:45 AM — 11:15 AM
SESSION 7 (CONTINUED): RESOURCING11:15 AM — 12:45 PM
SESSION 8: STUDY PREPARATION12:45 PM — 1:45 PM
1:45 PM — 2:45 PM
SESSION 9: IMP MANAGEMENT2:45 PM — 3:45 PM
SESSION 10: STUDY COMMUNICATION3:45 PM — 4:15 PM
4:15 PM — 5:00 PM
SESSION 10 (CONTINUED): STUDY COMMUNICATION8:30 AM — 10:15 AM
SESSION 11: SITE MANAGEMENT10:15 AM — 10:45 AM
10:45 AM — 11:45 AM
SESSION 12: EVALUATION AND REPORTING11:45 AM — 12:30 PM
SESSION 13: DRUG SAFETY12:30 PM — 1:30 PM
1:30 PM — 2:30 PM
SESSION 14: RISK MANAGEMENT2:30 PM — 3:30 PM
登録申し込み方法
Registration fee includes refreshment breaks, lunch on the 1st day of the course and training course material.
For bank transfer payment please use the printable registration form which is available at the back of the programme (click on View PDF below).
This course has limited capacity. Register early!