Annual Conference

Explore key CDM topics in greater depth

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  • Paulina Linares
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Explore key CDM topics in greater depth

One day before the SCDM 2022 Annual Conference kicks off, we are excited to offer you the possibility to join Pre-Conference Workshops that will allow you to explore key CDM topics in greater depth.

The Pre-Conference Workshops are interactive 4-hour long sessions run by practitioners and leading global education organizations. These sessions will provide a hands-on learning experience that will enable you to gain new insights and explore new strategies and tools in your day-to-day work.

What is more, you will earn 4.0 CEU’s/session after the successful completion of each workshop and respective assessment.

AI and Machine Learning: What it is and its Impact on Data Management

📅 Sunday, September 11 | 8:00 AM to 12:00 PM
💬 Instructor: Prasanna Rao, Senior Director & Global Head of AI/ML, Pfizer

SDQ-Smart Data Quality hands-on workshop will provide participants an immersive experience to work with state-of-the-art AI system in order to explain how Artificial Intelligence, Machine Learning and Rule engine work together along with human experts to reconcile Clinical Trial data.
Learn more.

Clinical Site Immersion

📅 Sunday, September 11 | 8:00 AM to 1:00 PM
💬 Instructor: Meredith Nahm Zozus, Professor, Div. Chief, Director Clinical Research Informatics, Univ. of Texas Health Science Center San Antonio

Most Data Managers have never seen a clinical investigational site. Don’t be that Data Manager!

Enrich your knowledge of clinical operations and data collection by experiencing operations at a live Clinical Research Site at the University of Texas Health Science Center at San Antonio. In this half-day workshop, attendees will tour the site and gain a greater understanding of site processes from study feasibility analysis, institutional site start-up, recruitment, study conduct and data collection.
Learn more.

Data Requirements for an FDA Submission

📅 Sunday, September 11 | 1:00 PM to 5:00 PM
💬 Instructor: Dan Crawford, Senior Director, Veeva Systems

This session will provide an overview of the requirements for submitting standardized electronic data and documents to Regulatory authorities (FDA, PMDA). We will also highlight some of the tools the FDA uses to facilitate their review and their approach to reviewing the safety and efficacy portions of a submission.
Learn more.

Author: Paulina Linares

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