Food, Supplements, and Cosmetics Regulatory

Experts You Can

Rely On

Get access to vetted regulatory professionals to support FDA compliance, submissions, and market entry — project-based, confidential, and outcome-focused.

3D illustration of an FDA approved rubber stamp with a checkmark and 'FDA Approved' text.

Our Service

Our team supports companies of all sizes in navigating U.S. and China FDA regulations, while also helping beverage brands from China and Asia enter the U.S. market—from concept to full commercialization.

GRAS Determination & Notification

  • Ingredient safety assessment
  • GRAS dossier preparation
  • Independent expert panel support
  • FDA Submission and questions response

New Dietary Ingredient (NDI) Notification

  • NDI eligibility assessment
  • FDA submission preparation
  • Risk review & response strategy

Beverage Turnkey Solution

  • Regulatory strategy for beverages
  • Formula & label compliance
  • Market entry readiness

Label Reviews&Compliance

  • Nutrition Facts & Supplement Facts review
  • Claims substantiation
  • FDA & FTC compliance check

FSVP Compliance Serivces

  • FSVP program setup
  • Supplier verification & documentation
  • FDA inspection readiness

FDA Facility Registration

  • Food facility registration
  • US agent support
  • Renewal & compliance monitoring

INCI Name Application

  • Ingredient classification & review
  • INCI name submission
  • Liaison with PCPC / regulatory bodies

China NMPA Registration & Filing

  • Regulatory pathway assessment
  • Ingredient & formula review
  • Registration / filing documentation support

Other Service

FEMA GRAS, CAS number support, and additional regulatory services for food, drugs, dietary supplements, cosmetics, and medical devices.

How It Works

1. Submit Your Project
Tell us your regulatory challenge, product type, and timeline.

2. Get Matched with Vetted Experts
We match you with FDA and industry-experienced specialists based on your specific needs.

3. Deliver with Confidence
Projects are managed with clear scope, milestones, and confidentiality safeguards.

Why EZFDA

  • Experts vetted for real FDA and regulatory experience
  • Project-based engagement — no long-term commitments
  • Confidential and NDA-protected collaboration
  • Platform-managed scope and quality oversight
  • Focused exclusively on food, supplements, and cosmetics

Find Your Expert

Start with a regulatory conversation — not a sales pitch.

Submit your project and we’ll get back to you within 48 hours.

Check your ingredient’s current U.S. FDA regulatory status in seconds.