EZFDA Consulting, ndi notice, gras NOtice, Inci, NMPA
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EZFDA Consulting
Expertise You Can Rely On
EZFDA Consulting, ndi notice, gras NOtice, Inci, NMPA
Expertise You Can Rely On
Our team supports companies of all sizes in navigating U.S. and China FDA regulations, while also help beverage brands from China and Asia enter the U.S. market—from concept to full commercialization.
Our team of experts can help your company navigate the scientific and regulatory requirements for supporting the GRAS status of your ingredients.
Need help to submit new dietary ingredient notification (NDIN)? Our team is here to provide you quick and professional help.
Our team have the experience to develop and evaluate your compliance FSVP plans and are ready to assist any international or domestic food companies developing and implementing FSMA-critical food safety plans.
Ask our expert to check your food, supplement, alcoholic and non-alchonolic beverage labels for regulatory compliance.
At EZFDA, we specialize in helping global beverage brands—both alcoholic and non-alcoholic—successfully enter and thrive in the U.S. market. From product concept and formulation to co-packer selection and regulatory compliance, our turnkey solutions cover every step of your journey.
Get help with food, drug, dietary supplement, cosmetic, or medical device services.
At EZFDA Consulting Inc, we have extensive experience in FDA regulatory affairs, providing expert guidance and support to clients across a wide range of industries. Our team of skilled professionals has a deep understanding of FDA regulations and stays up to date on the latest trends and changes. We have successfully assisted clients with
At EZFDA Consulting Inc, we have extensive experience in FDA regulatory affairs, providing expert guidance and support to clients across a wide range of industries. Our team of skilled professionals has a deep understanding of FDA regulations and stays up to date on the latest trends and changes. We have successfully assisted clients with filing, GRAS application, FSVP planning, NDI filing, and related services for the US FDA regulations. Our experience has allowed us to develop a comprehensive understanding of the regulatory landscape and how to navigate it effectively.
Our team at EZFDA Consulting Inc is made up of experienced professionals who bring a diverse range of skills and expertise to the table. With backgrounds in R&D, QA, QC, regulatory affairs, and FDA work experience, our team has the knowledge and skills needed to help our clients achieve regulatory compliance. Most of our team members hold
Our team at EZFDA Consulting Inc is made up of experienced professionals who bring a diverse range of skills and expertise to the table. With backgrounds in R&D, QA, QC, regulatory affairs, and FDA work experience, our team has the knowledge and skills needed to help our clients achieve regulatory compliance. Most of our team members hold a PhD degree, and we are proficient in English and multiple languages, including Chinese, Vietnamese, and more. We work collaboratively to provide customized solutions that address the unique needs of each of our clients.
Navigating the complex regulatory landscape of the FDA can be challenging, but at EZFDA Consulting Inc, we make it easy for our clients. We are committed to providing expert guidance and support, customized solutions, and efficient service. We tailor our services to meet the specific needs of each of our clients, regardless of the size or
Navigating the complex regulatory landscape of the FDA can be challenging, but at EZFDA Consulting Inc, we make it easy for our clients. We are committed to providing expert guidance and support, customized solutions, and efficient service. We tailor our services to meet the specific needs of each of our clients, regardless of the size or scope of their operations. Our team of professionals is dedicated to helping our clients achieve regulatory compliance and maximize success in the marketplace. With our expertise, efficiency, and bilingual support, we are the premier choice for FDA regulatory affairs services.
EZFDA consulting
400 West Capitol Avenue, Suite 1700, Little Rock, AR, 72201
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