Bridging Chinese brands to US FDA compliance with speed and clarity.
KECC Consulting LLC was founded in 2026 in Tustin/Irvine, California with a clear mission: make FDA regulatory compliance accessible, fast, and affordable for brands entering the US market — especially those bridging China and the United States.
We saw too many brands struggle with opaque consulting fees, weeks-long turnarounds, and language barriers. KECC was built to change that — combining deep regulatory expertise with efficient, people-first workflows to deliver compliant results at a fraction of the traditional cost and time.
Whether you're launching a supplement on Amazon, registering a cosmetic facility under MoCRA, or navigating a 510(k) submission for a medical device, KECC is your bilingual compliance partner.
FDA Regulatory Research & Compliance Analyst
B.S. Biology from UC Irvine. Calvin conducts regulatory research, reviews labels and product formulations, and ensures every deliverable meets FDA requirements.
Director of Regulatory Affairs
Cheng Eric Chang oversees all regulatory strategy at KECC. With deep expertise in FDA compliance, Eric ensures our consulting meets the highest standards of accuracy and professionalism.
KECC's team of experienced regulatory professionals handles every project with precision and care — from label reviews to compliance reports and gap analyses.
When you submit a project, our regulatory specialists immediately begin a thorough review based on FDA regulations, your product details, and our proprietary compliance frameworks. Every document is carefully prepared and finalized by our team before delivery.
The result? You get expert-quality deliverables in days instead of weeks — at a price that makes compliance accessible to startups and small brands, not just Fortune 500 companies.
FDA Regulatory Advisor · KECC