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Hotel Grand Majestic Plaza

2018 年 02 月 26 日 8:00 上午 - 2018 年 02 月 27 日 12:15 下午

Truhlarska 16, 110 00 Prague 1, Czech Republic

EU-RMP Creation

The participants will learn the best practice in medical writing of the EU-RMP. The solutions will be demonstrated in practical exercises included throughout the course.

会议日程

8:00 AM8:30 AM

REGISTRATION

8:30 AM8:45 AM

WELCOME AND INTRODUCTION OF FACULTY AND PARTICIPANTS

8:45 AM9:15 AM

INTRODUCTION TO BENEFIT-RISK MANAGEMENT

9:15 AM10:00 AM

OBJECTIVES AND STRUCTURE OF THE EU-RMP

10:00 AM10:30 AM

COFFEE BREAK

10:30 AM11:15 AM

GROUP WORK - PROJECT MANAGEMENT

11:15 AM12:00 PM

SOURCE DATA AND PLANNING PROCESS

12:00 PM1:00 PM

LUNCH

1:00 PM1:30 PM

PRODUCT AND DISEASE/CONDITION OVERVIEW

1:30 PM2:15 PM

SAFETY SPECIFICATION MODULES SII-SVI

2:15 PM2:45 PM

COFFEE BREAK

2:45 PM4:15 PM

IDENTIFIED/POTENTIAL RISKS AND SAFETY CONCERNS (MODULES SVII AND SVIII)

4:15 PM4:45 PM

PHARMACOVIGILANCE PLAN AND POST-AUTHORISATION EFFICACY STUDIES

4:45 PM5:45 PM

NETWORKING RECEPTION

8:00 AM8:45 AM

RISK MINIMISATION PLAN

8:45 AM9:30 AM

SUMMARY OF THE EU-RMP AND ANNEXES

9:30 AM10:00 AM

EXERCISE ON IDENTIFICATION OF SAFETY CONCERNS

10:00 AM10:30 AM

COFFEE BREAK

10:30 AM12:00 PM

GROUP WORK - WRITING EXERCISE

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