Regulatory Affairs Part I: The IND Phase

15 - 17 March 2010, Horsham, United States

Introduction

Learn how to apply regulatory concepts to ensure compliant IND submissions to FDA. The course focuses on drug and well characterized biological products and not the regulatory process for devices, generic products, or traditional biologics.

Venue

Drug Information Association, Inc.

Drug Information Association, Inc., Horsham, 19044, United States

Organised by

DIA

Contact information

UU裸聊直播

Share:

Regulatory Affairs Part I: The IND Phase

15 - 17 March 2010, Horsham, United States

Search

Exclude Online events

Select date range

Start Date

End Date

Location

Subject area

Event type