Regulatory Affairs: The IND, NDA, and Post-Marketing

Attend this live, virtual training course to learn about FDA regulations and expectations for the content, submission and review of INDs and NDAs, and the importance of regulatory strategy.

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Regulatory Affairs: Part 1: The IND – Investigational New Drug Application

Session Chair(s)

Carol H. Danielson, DrPH, MS, RAC

President

Regulatory Advantage, LLC, United States

Kevin Daniel Healy, PhD

Senior Vice President Regulatory Affairs

Entrada Therapeutics, United States

Regulatory Affairs: Part 1: The IND – Investigational New Drug Application

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Regulatory Affairs: The IND, NDA, and Post-Marketing

Regulatory Affairs: Part 1: The IND – Investigational New Drug Application

Session Chair(s)

Carol H. Danielson, DrPH, MS, RAC

Kevin Daniel Healy, PhD

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