The Mechanics of Clinical Trial Agreements

Foley Partner Janice Anderson and Associate Leeann Habte are speaking at the Association of Clinical Research Professional's (ACRP) 2008 Workshop Weekend, October 11 - 12, 2008 in Las Vegas, Nevada.

Ms. Anderson and Ms. Habte are presenting on October 12, 2008 from 8:00 a.m. - 12:00 p.m. on "The Mechanics of Clinical Trial Agreements."

We will analyze a typical clinical trial agreement to address the financial, clinical, ethical, regulatory, and legal issues addressed by each component from a fiscal, clinical, and regulatory perspective. For example, the requirements of HIPAA authorization and consent representations and warranties, indemnification clauses, governing law clauses, how to negotiate a budget, etc.

Upon completion of this program, attendees should be able to:

• Identify the key structural components of a compliant clinical trial agreement.
• Negotiate a budget with consideration of regulatory objectives.
• Spot problem areas or issues that address special attention.

For more information please visit ACRP's Web site.