Deemed Product Review: A Conversation with the Center for Tobacco Products Office of Science

On this page:

• Meeting Objective
• Agenda
• Meeting Materials
• Additional Resources

Meeting Objective

This meeting was intended to provide information on the scientific review of applications received by Sept. 9, 2020. The meeting focused on the application intake process, review progress, and allocation of review resources, and included time for audience questions. The meeting was not intended to communicate any new policies or interpretations regarding tobacco product marketing applications and their review.

Agenda

This live, virtual meeting featured a presentation from CTP Office of Science Director Matt Holman and included a question and answer session with Office of Science staff.

1:00 pm – Opening Remarks and Overview of the Meeting — Anne Radway, M.S., CTP Office of Science

1:15 pm – Presentation: Deemed Product Review — Matthew R. Holman, Ph.D., Director, CTP Office of Science

2:00 pm – Question & Answer Session

Moderator: Anne Radway, M.S., CTP Office of Science

Panelists:

• Matthew R. Holman, Ph.D., Director, CTP Office of Science
• Todd L. Cecil, Ph.D., Deputy Director for Regulatory Management, CTP Office of Science
• Crystal Allard, Director, Division of Regulatory Science and Informatics (DRSI), CTP Office of Science
• Joanna C. Randazzo, D.C., Chief (Acting), Science Policy Branch, CTP Office of Science
• Cristi Stark, M.S., Director, Division of Regulatory Project Management (DRPM), CTP Office of Science

Meeting Materials

• Transcript
• Presentation Slides

Additional Resources

• Market and Distribute a Tobacco Product
• Perspective: FDA’s Progress on Review of Tobacco Product Applications Submitted by the Sept. 9, 2020 Deadline
• Tobacco Product Applications: Metrics & Reporting
• Deemed New Tobacco Product Applications List