Manufacturers whose products are being reviewed may submit clinical information to the Drugs and Therapeutics (D and T) Committee and the Department. Manufacturers should submit a concise synopsis of their product.  This synopsis should be no more than four pages in length.  The Committee is particularly interested in information that sets a drug apart from other drugs in its class or PDL category.  The Committee is not interested in materials intended to market a product.  For information on the process for submitting clinical information to the D and T Committee, manufacturers should contact Ken Ryan at the Illinois State Medical Society at ryan@isms.org. Clinical information may also be submitted to the department’s clinical contractor at:

Mary Lynn Moody, BSPharm
Director, Drug Information Center
Clinical Assistant Professor
Department of Pharmacy Practice
University of Illinois at Chicago
College of Pharmacy
833 S. Wood Street
Chicago, Il 60611
312-996-2351
mlmoody@uic.edu