The Experts in FDA and USDA Regulatory Matters
EAS Consulting Group is a leading provider of regulatory compliance solutions to industries regulated by FDA, USDA, and supporting agencies. Our team of consultants provide expert guidance for all of your regulatory requirements.
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Our Services: Consulting • Submissions • Auditing • Training • Legal Support
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Seminars
Claims Substantiation Seminar
Presented by Paula Brock, PhD., EAS Senior Regulatory ConsultantNew Date Coming Soon 1:00 – 3:00PM (Eastern)It is required in the United States that manufacturers and other advertisers of dietary supplements such as distributors, retailers, and endorsers, have...
Webinars
21 CFR Part 11 and FDA Compliance
Risk-Based Approach to CSV, 21 CFR Part 11 and FDA ComplianceAn EAS Consulting Group Complimentary WebinarPresented by Carolyn Troiano, EAS Independent ConsultantNovember 8, 2024 • 1:00 PM – 4:00 PM (Eastern)Enter Your Information to Watch NowBy clicking submit above,...
On Demand Webinars
Claims Substantiation of Cosmetic Products
An EAS Consulting Group Complimentary On Demand WebinarPresented by Paula Brock, Ph.D., MCSISeptember 9, 2024 • 11:30 AM (Eastern) • Length: 45 minutesSubstantiation of product claims is required by law in the USA and this is not different for cosmetics. All types of...
Latest News
CVM GFI #294 – Animal Food Ingredient Consultation (AFIC)
The Federal Food, Drug, and Cosmetic Act (FD&C Act) gives FDA the authority to regulate substances used in animal food, including substances that are food additives and substances that are...
Important Changes to OTC Monograph Listing Marketing Categories
In addition to a reminder of the Drug Establishment Registration Renewal period (1 October – 31 December) EAS would like to remind you of significant changes being implemented for OTC monograph drug...
Investigating Pesticide Tolerance
By Dr. Bill Reeves, EAS Regulatory ConsultantConsistent, scientifically justified regulations enable over $1.5 trillion in global agricultural exports every year. The world economy depends on these...
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EAS – Your Dedicated Consultant for FSVP Services
EAS offers comprehensive services related to FSMA’s FSVP program for both foods and dietary supplements. We can even act as your Qualified Individual. For more information about our services, watch our short video.
Dietary Supplement Good Manufacturing Practice Compliance Short Course
The GMPs dictated in 21 CFR 111 have been in place for over a decade, but the FDA continues to issue numerous Warning Letters for a failure to comply with even the basic tenets of the regulation. EAS Consulting Group’s two-part short course covers the basics of working in a GMP environment including personal hygiene, sanitation, the use of SOPs, and Good Documentation Practices (GDPs). It also addresses the top 5 observations cited in FDA Warning Letters since 2010 which are Specifications, Master Manufacturing and Batch Production Records, Quality Unit responsibilities, Product Complaints, and Holding and Distribution Operations.
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