REGULATORY COMPLIANCE
EAS Consulting Group
EAS Consulting Group is one of the largest FDA regulatory consulting firms in the United States, with a network of over 200 independent consultants specializing in dietary supplement, food, drug, medical device, and cosmetic compliance. A Certified Group company, EAS provides comprehensive consulting, training, and auditing services for DSHEA compliance, 21 CFR Part 111 GMP requirements, label and claims review, New Dietary Ingredient (NDI) notifications, and FDA inspection preparation. Their consultant network includes former FDA investigators and industry quality experts who conduct GMP audits, mock inspections, and gap analyses.
Alexandria, Virginia
Directory Listing · Records Reviewed
Public records and independent sources have been reviewed.
What this means →- MOQMOQ (Minimum Order Quantity)The smallest production run a manufacturer will accept for an order.
- Project-based (consulting)
- LEAD TIMELead TimeThe time from order placement to finished product delivery.
- Not publicly disclosed
§1Editorial assessment
EAS Consulting Group is one of the largest FDA regulatory consulting firms in the United States, with a network of over 200 independent consultants specializing in dietary supplement, food, drug, medical device, and cosmetic compliance. A Certified Group company, EAS provides comprehensive consulting, training, and auditing services for DSHEA compliance, 21 CFR Part 111 GMP requirements, label and claims review, New Dietary Ingredient (NDI) notifications, and FDA inspection preparation. Their consultant network includes former FDA investigators and industry quality experts who conduct GMP audits, mock inspections, and gap analyses.
§2Six-gate readout
Six gates we apply before any name appears in the directory. Each gate is auto-derived from public evidence on this profile.
§3Inspection history
§4Certifications
0 of 1 certification independently confirmed. What this means
§5Capability matrix
- PRODUCT TYPES
- GMP Consulting · Label & Claims Review · NDI Notifications · FDA Inspection Prep · Training Programs
- CAPABILITIES
- 21 CFR Part 111 Compliance · GMP Auditing & Gap Analysis · Mock FDA Inspections · Structure/Function Claim Substantiation · Quality System Development · Stability Program Development · Adverse Event Reporting · US Agent Services
§6Sources
- EAS Consulting Group Official Website(2026-03-13)
- EAS Dietary Supplement Services(2026-03-13)
- EAS About Us(2026-03-13)
- EAS Supplement Training Programs(2026-03-13)
Dietary supplement manufacturers must comply with 21 CFR Part 111 (Current Good Manufacturing Practice for dietary supplements). This includes requirements for personnel, facilities, equipment, production, laboratory operations, and record-keeping.
Disclosures
- No material connection exists between Inventory Ready and this company
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