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Bethesda North Marriott Hotel and Conference Center

2024年2月12日 (月) 午前 8:00 - 2024年2月14日 (水) 午後 2:30

5701 Marinelli Road, North Bethesda, MD 20852

Regulatory Submissions, Information, and Document Management Forum

Session 2: FDA Plenary: Data and Technology Strategy

Session Chair(s)

Ethan  Chen, MBA, MS, PMP

Ethan Chen, MBA, MS, PMP

Director, Division of Data Management , FDA CDER, United States

During this session presenters will cover a variety of topics about the FDA Data and Technology Strategy. Topics will include Next Generation of the Electronic Submissions Gateway, data quality challenges in regulatory submissions, and CBER updates.

Learning Objective : At the conclusion of this session, participants should be able to:
  • Discuss current FDA data quality challenges in regulatory submissions and identify areas of improvement to submit better quality data for FDA review
  • Describe the details that encompass the next generation of the electronic submissions gateway in the cloud
  • List and explain selected key data standards initiatives in CDER and CBER

Speaker(s)

Sri  Mantha, MBA, MS

Sri Mantha, MBA, MS

Acting Chief Information Officer, FDA, United States

Data Quality Challenges in Regulatory Submissions and Their Impact

Jessica  Bernhardt, MS

Jessica Bernhardt, MS

IT Project Manager ODT, FDA, United States

Electronic Submission Gateway Next Generation (ESG NextGen)

Ginny  Hussong

Ginny Hussong

Branch Chief, Data Standards, CBER, FDA, United States

CBER Updates

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