Share:

Regulatory Affairs: Part 1: The IND Phase

21 - 23 September 2011, Horsham, United States


Introduction
All You Need to know about IND Submissions in Only 3 Days



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.

Event Code:
11434
Venue
Drug Information Association, Inc.

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

Organised by
DIA
Contact information
Susan Mazak
215.442.6183
Contact us by email

Search
 
 
Showing all upcoming events
Start Date
End Date
Location
Subject area
Event type

Advertisement
Spotlight


E-mail Enquiry
*
*
*
*