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

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

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Introduction to Regulation of Drugs and Biologics in the United States: Pre-Course Part One

Session Chair(s)

Drusilla Scott, PhD, RAC

Vice President, Regulatory Affairs

Sobi, Inc., United States

Introduction to Regulation of Drugs and Biologics in the United States: Pre-Course Part One

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

Introduction to Regulation of Drugs and Biologics in the United States: Pre-Course Part One

Session Chair(s)

Drusilla Scott, PhD, RAC

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