Effectively Managing Multi-Center Clinical Trials

Presented by the Indiana Medical Device Manufacturers Council

January 27, 2011

CLE Hours have been Requested

Presented by:

Jennifer L. Kerr, VP, Operations, MED Institute, Inc.
Gretchen Miller Bowker, RAC, COO, Pearl IRB, LLC
Jenna Sallee, Executive Director, Orthopaedic Research Foundation Inc.

Sponsorship Available

Program Overview

This IMDMC Regulatory Roundtable will feature knowledgeable leaders in their field focusing on key issues confronted by all parties when managing larger clinical trials. The most common issues encountered and best practices needed for successful larger scale, multi-site studies will be discussed including:

1. Clinical Site Issues
2. Sponsor or CRO Issues, and
3. Regulatory IRB Issues
All followed by detailed Q&A

Register Online at http://www.imdmc.org!

Registration: 11:30 am

Lunch Included: 12:00 pm

Program 12:30 – 2:30 pm

Location: Montage Catering Facility, 8580 Allison Pointe Blvd., Indianapolis, IN 46250

Members: $65 per person

Non-Members: $80 per person

For more information:
Contact: Blake Jeffery
Phone: 317-951-1388
Email: IMDMCoffice@ameritech.net

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