Congressional Testimony

Congressional Testimony

The reprocessing industry has a long history of stringent legislative and regulatory oversight and examination.  Excerpts from statement of Daniel Schultz, M.D., Director, Center for Devices and Radiological Health, Food and Drug Administration (FDA), before the Committee on Government Reform, House of Representatives on September 26, 2006. Dr. Schultz’ full testimony.

Testimony submitted to the Senate Health, Education, Labor and Pensions Committee (HELP) for its hearing on reuse, June 27, 2000:

Testimony submitted to the House Energy and Commerce Subcommittee on Oversight and Investigations for their hearing on reuse held February 10, 2000:

AHA’s Written Testimony, presented by Dr. Walter G. Maurer of The Cleveland Clinic