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About

Our mission is to provide quality regulatory advice and service and to represent the best interests of our clients in an ethical, timely, and cost efficient manner. Description EAS Consulting Group, LLC (EAS) specializes in Food and Drug Administration (FDA) regulatory matters. Our prime focus is to assist domestic and foreign pharmaceutical, medical device, tobacco, food, dietary supplement, and cosmetic firms comply with applicable laws and regulations. EAS is staffed with former FDA compliance and inspection officials and industry executives, and is assisted by an extensive network of consultants with many years of FDA and industry experience. Headquartered in Alexandria, VA with consultants and auditors located strategically throughout the U.S., EAS Consulting Group was established as an independent company in October 2006. Prior to that, it was a division of Kendle Regulatory Affairs (formerly known as AAC Consulting Group). The company’s roots go back nearly a half century to 1960 when Arthur A. Checchi, former FDA Associate Commissioner, founded the company. In 1985 FDA’s Director of Regional Operations, Anthony C. Celeste, assumed the leadership of the company. He operated it under the name AAC Consulting Group (AAC). In 2001 the company was acquired by Kendle International, one of the world’s largest global clinical research organizations. In 2006 Mr. Steele, then President of AAC and Vice President of the company’s Regulatory Affairs, acquired the Division of Food, Dietary Supplement, and Cosmetic Consulting from Kendle. At that time he formed EAS Consulting Group as an independent company. In September 2007, pharmaceutical, medical device consulting was added to the list of services offered by EAS.