We are pleased to invite you to a half-day seminar where you will learn how to facilitate trial safety and efficacy with automated reporting tools, roll-based workflows and clinical analysis capabilities including risk-based monitoring, data monitoring and fraud detection.
Date: Tuesday May 23rd, 2017
Time: 10:00 – 13:30
Venue: Medicon Village, Scheelevägen 2, 223 63 Lund, Sweden – Auditorium
The seminar is FREE, but please make sure to register:
Medical writers and clinical data scientists will learn how to:
- Automate significant portions of the clinical study reporting process, reducing the time and complexity underlying adverse event narrative submission.
- Build summary dashboards to help evaluate safety and efficacy issues in a single click.
- Generate customised patient narratives and patient profiles.
Data managers and clinical operators will learn how to:
- Minimise data quality risks with risk-based monitoring tools in JMP Clinical that make it easy to identify outliers and data anomalies at any level of the organisation.
- Isolate factors responsible for data integrity issues.
- Ensure data quality with visualisations that make it easy to identify modified or duplicate data.
PROGRAM
|
10:00 |
Registration and Coffee |
|
10:30 |
Introduction |
|
10:40 |
Learn how Clinical Data Scientists support trial safety and efficacy data for validity, monitoring and submission |
|
11:20 |
Break |
|
11:50 |
Learn how Data Management and Clinical Operations work together using visualization and algorithms in ongoing |
|
12:30 |
Conclusion |
|
12:40 |
Networking Lunch |
SPEAKERS
 |
 |
| Richard C. Zink JMP Principal Research Statistician Developer, SAS |
Valerie Nedbal JMP Senior System Engineer |
IN COLLABORATION WITH
VENUE SPONSOR:
