EAS Consulting Group, LLC (EAS) is a leading provider of FDA regulatory consulting services, with over 50 years of experience in helping firms to navigate applicable laws and regulations. We have assisted thousands in all matters of FDA regulatory issues, from performing cGMP audits and mock FDA inspections, quality system implementation and remediation, product development and regulatory strategies, to submissions, filings, registrations, assistance with imports and acting as a US Agent. As a member of the Certified family of companies, EAS is able to provide regulatory solutions, testing and guidance with a commitment to compliance, quality systems and technical expertise.
EAS offers over 150 independent consultants, specialists in their fields and former FDA officials and high-level industry executives, who provide unparalleled expertise pertaining to your specific needs. Visit our website, www.easconsultinggroup.com to learn more about our consulting and auditing services or our industry services pages for a quick overview of EAS regulatory scope of services. We offer a wide-variety of complimentary compliance webinars on regulatory topics of interest to GRMA members and all of our news and articles can be found on our EAS blog. Contact us for more information and receive the monthly EASeNews in your inbox