Norton Audits Inc to Train US Food and Drug Administration Complaint Management and Advanced Interviewing Techniques the Second Class Conducted by NAI for the FDA



May 5, 2005 -- The FDA's Center for Devices and Radiological Health (CDRH) is responsible for overall product approval, product safety, consumer protection, and oversight of biomonitoring activities for all medical device products approved by the FDA. Norton Audits' selection was based on fifteen years of clinical data auditing expertise, unyielding compliance law experience, national training reputation, and regulatory case development skills in both the medical device and pharmaceutical industries.

Additionally, Norton Audits announced preparations for Tamera Norton Smith to jointly present with the U.S. FDA at the 2006 Association of Clinical Research Professionals (ACRP) National Conference to be held in Phoenix, Arizona. The Center of Devices and Radiological Health has set the topic for 2006 to address Quality Systems in Clinical Trials.

About Norton Audits, Inc.:
Norton Audits' mission continues to focus on advancing clinical research through strategic systems development and implementation for defining and driving performance excellence. Norton Audits' most successful product is their skill set for identifying and helping their clients proactively identify and limit their risk that would prevent an approval of a New Drug Application and Medical Device Pre-Market Application. Norton Audits provides auditing, monitoring, consulting and training services and products to the Clinical Research Industry. Norton Audits, Inc. is also a member of the University of South Carolina Technology Incubator.

For more information, please visit www.nortonaudits.com.





Norton Audits Inc to Train US Food and Drug Administration Complaint Management and Advanced Interviewing Techniques the Second Class Conducted by NAI for the FDA