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Specializing in FDA Regulatory Matters

EAS Consulting Group Enters Into an Asset Purchase Agreement with Phoenix Regulatory Associates

January 12, 2016

For Immediate Release
Media Contact: Cathryn Sacra (571) 447-5500

Alexandria, VA: EAS Consulting Group, LLC., (EAS) is pleased to announce that it has entered into an agreement to continue to provide regulatory services to Phoenix Regulatory Associates, Ltd., clients upon the closure of Phoenix after nearly a quarter century of operation. “Phoenix has been a leader in providing similar services as EAS to the full spectrum of industries regulated by FDA, so the transition to EAS will be seamless. We are delighted that such a reputable firm would entrust the continued care of their clients to us and wish Phoenix partners, CK Gund and Clyde Takeguchi, well in their retirement” says Edward Steele, EAS Chairman & CEO.

EAS is well known for having one of the largest and most experienced consultant networks in the industry, with approximately 150 technical experts in the areas of foods, pharmaceuticals, dietary supplements, medical devices, biologics, cosmetics and tobacco. Many additional consultants who had previously worked with Phoenix clients are now joining EAS ranks, expanding that expert network even further.

FDA’s many compliance requirements often make the hiring of a consultant invaluable to industry. Companies find the ability to draw on this expertise as needed a beneficial tool that boosts their regulatory capabilities. At EAS, our goal is to provide the most thorough guidance in the most cost effective manner. We work hard to ensure client’s needs are met and that gaps are identified and evaluated in a solutions driven environment.

EAS’s regulatory consultants are former high-level Food and Drug Administration officials and industry executives, experts in their fields, providing peace of mind for businesses working hard to protect the health and safety of the American consumer.

About EAS Consulting Group, LLC

EAS Consulting Group specializes in FDA regulatory matters in the dietary supplement, pharmaceutical, medical device, food, tobacco, biologic and cosmetic industries, including assistance in tailored compliance trainings, 483 responses, mock-FDA audits, labeling compliance and more. EAS is staffed with former industry experts and FDA officials who have expertise in both FDA policies and enforcement.

More information can be found on the EAS website, 

or by contacting Cathryn Sacra at (571) 447-5500