Pre-Symposium Sessions
 

Consider registering for one of the two concurrent sessions organized by the U.S. Food and Drug Administration.  Both sessions begin at 1:00 p.m. Eastern Time on Tuesday, June 7 and will last approximately four hours.  One may register for a pre-symposium session without registering for the main symposium.

Human Factors Validation of Combination Drug Products: An FDA Workshop

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This session provides a forum for an interactive dialog between the FDA/CDER human factors team and sponsors, consultants and other interested persons regarding human factors (HF) validation of combination drug products. Participants will have opportunities to ask questions to the presenters.

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Oluwamurewa (Murewa) Oguntimein, Human Factors Team Leader, DMEPAI

Jason Flint, Associate Director for Human Factors, DMEPAI

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Improving the Safety and Effectiveness of Medical Devices Through Human Factors Considerations: An FDA Interactive Session

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This interactive forum provides a forum for an interactive dialog between FDA/CDHR human factors team and sponsors, consultants and other interested persons regarding human factors (HF) validation of a variety of medical device and systems. Participants will have opportunities to ask extensive questions to the presenters.

Janine Purcell Human Factors Reviewers, FDA/CDRH/OPEQ

Hannniebey Wiyor, PhD, Lieutenant, USPHS

Kimberley Kontson, FDA CDRH

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Early fees in effect until May 20, 2022.

To register for a pre-symposium session only without registering for the main symposium.

Click the Register Now button above to login to your account or to create an account.

To register for a pre-symposium session and the full symposium, or to register for the full symposium only.  (Separate fees apply for the June 7 pre-symposium sessions and the June 8 & 9 symposium)

Click the Register Now button above to login to your account or to create an account.