ON-DEMAND WEBINAR · November 7, 2019 - Held in Chinese
Data validation – Why, What and How in the context of new technology
- Session Overview: Data validation is one of the key activities and critical process to ensure good data quality for a clinical trial.
Overview
Data validation is one of the key activities and critical process to ensure good data quality for a clinical trial. Defining the data validation strategy depends on data requirements, fit-for-purpose quality. In addition, data validation is a cross-functional activities and heavily rely on the EDC system functionality and other tools. New technology landscape helps improve the efficiency of data validation. During this webinar, the Instructor will introduce:
1 - Data management assumption
- a) Data requirements (ALCOA, CCEA, FAIR)
- b) Fit-for-purpose data quality
2 - Data validation strategy
- a) Cross-function collaboration
- b) Type of data validation
- c) Strategy and considerations
3 - Technology advancement helps data valuation (smart DB setup, visualization etc.)
What You'll Learn
- Understand the data management assumptions and the data requirement (present and future)
- Understand the data validation strategy and considerations
- Understand how the technology advancement could improve data validation
Who Should Attend
Data Managers with intermediate through advanced levels of experience with determining Data validation checks and metrics. Participants will benefit from this Webinars' review of current Data Validation methodologies.
Better understand how the technology improve data validation and learn more about data validation strategy and consolidation.
Meet the Speaker
Stella Gu
Senior Data Manager, Roche (China) Holding Ltd.
Stella Gu, serves as Senior Data Manager in Roche (China) Holding Ltd. She graduated from Tongji University with master degree of Biomedical Engineering. Stella has 8 years’ experience in clinical data management as study coordinator and study data manager in Global Medical Consulting services, Quintiles and Roche. Stella is the expert in using different EDC systems, including Rave, Oracle, OC-RDC, InForm, and familiar with different reporting tools, such as I-Review, J-Review, Hyperion and Spotfire. Besides, she has one year’s experience of study management in clinical operation team, managing internal and external partners. Stella has deep understanding on the drug development and project management, and has unique insights on data management.
Earn CEUs
SCDM is authorized by IACET to offer 0.2 CEUs for this program. Participants are eligible to receive CEUs upon attendance and successful completion of a web-based assessment within 30 days after the webinar. CEUs are not granted after the 30-day assessment deadline.
Price
SCDM members: $50
Non-members: $175
Not yet an SCDM member? Purchase this conference session and get a one-year membership with SCDM on us to enjoy all our educational programs and sessions at a discounted price.
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