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Specializing in FDA Regulatory Matters

EAS Consulting Group, LLC Announces Timothy Stewart, Ph.D. as New Independent Advisor for Dietary Supplements

EAS Consulting Group, LLC is very pleased to welcome Timothy Stewart, Ph.D. as the new Independent Advisor for Dietary Supplements.  Dr. Stewart has been an Independent Consultant for EAS since 2013 and has proven to be an invaluable asset to dietary supplement clients, taking on the most challenging projects and providing sound solutions that offer a way forward in the complex world of dietary supplement FDA regulations.

Stewart is a Ph.D. in Chemistry, and an expert in applications such as raw material and finished product specifications, scientifically valid test methods, serious adverse event reporting, retail labeling, Prop. 65, Good Manufacturing Practices (GMPs). He is also an internationally recognized trainer with many by-name requests for in-house compliance training as well as industry trade shows. As a training facilitator Stewart specializes in Quality Control, Quality Assurance techniques, equipment/instrumentation IQ/OQ/PQ and also assists firms in developing and assuring appropriate testing procedures.

Dr. Stewart joins a team of EAS Independent Advisors who are leaders in their fields in developing regulatory compliant strategies, serving as expert witnesses and providing expert regulatory advice:

Edward A. Steele, EAS Chairman and CEO and Dean Cirotta, President and COO are pleased that EAS continues to provide high level technical consultation for clients, and feel the appointment of Dr. Stewart to Independent Advisor, continues to set EAS apart in its ability to provide pertinent leadership in the areas of FDA regulatory compliance. “We welcome Tim in his new advisory role,” says Dean Cirotta. “His expertise is an asset to EAS clients and we look forward to him expanding that role as he continues to work with us.”

About EAS Consulting Group, LLC

While EAS Consulting Group celebrates its tenth year of service under the name EAS, it continues to carry on 55 plus years of leadership in providing regulatory consulting to the industries regulated by FDA and other federal and state agencies. Our network of independent advisors and consultants enables EAS to provide comprehensive consulting, training and auditing services to the dietary supplement, pharmaceutical, food, medical device, tobacco and cosmetic industries. Whether the need is assistance with general FDA or USDA regulatory compliance or more specific needs such as product development, New Dietary Ingredient submissions, FSMA regulation compliance, generic or customized compliance trainings, 483 responses, product market withdrawals or recalls, mock-FDA audits, expert witness services, GRAS & food additive issues, dietary supplement labeling compliance or the development of a detailed import strategy and policy, EAS, with its over 150 consultants, former FDA compliance officials and industry experts, is able to assist. With vast expertise in FDA’s policies and enforcement, EAS is the proven choice for assistance in FDA and other regulatory matters.