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Seaport Hotel

Aug 12, 2019 7:45 AM - Aug 15, 2019 5:00 PM

One Seaport Lane, Boston, MA 02210

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

Learn about FDA regulations and expectations for the content, submission and review of INDs/NDAs, and the importance of regulatory strategy.

Back to Agenda

Session 2: The IND in Detail - Modules 1, 2, and 5

Session Chair(s)

Drusilla Scott, PhD, RAC

Drusilla Scott, PhD, RAC

Vice President, Regulatory Affairs

Sobi, Inc., United States

IND Item 1: Form FDA 1571
IND Item 2: Table of Contents
IND Item 3: Introductory Statement
IND Item 4: General Investigation Plan
IND Item 5: Investigator’s Brochure
IND Item 6: Protocols

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