Agreement to Terms and Conditions

By proceeding to make payment, you confirm that you agree to the following Terms and Conditions

The FDA registration is an add-on compliance, regulatory and technical service provided by EAS which enables us to monitor and review the registration status of your products with the U.S. FDA. The following terms must be noted for all FDA Services:

The parties agree that EAS shall review registration status of Client’s product with the U.S. Food and Drug Administration ("FDA")

EAS offers services across the globe for Food products, drugs and medical services etc . It remains the responsibility of the client to comply with all local laws and regulations while signing service agreements with EAS.

While offering regulatory services, EAS takes the utmost care to provide the right guidance that considers the Client Company’s welfare, and that is based on EAS’s knowledge and experience. Consulting services will not be held legally binding.

EAS is a private consulting firm and not associated with the FDA in any manner.

Client represents and warrants that it is the owner, operator or agent in charge of the identified product and will provide EAS with all information and materials necessary or reasonably requested by EAS to review the registration status of the product. Client warrants that the information and materials provided by Client will be accurate, truthful, genuine and current.

The services performed by EAS under this agreement are limited to those required to register Client. EAS’s fee shall be paid in accordance with EAS’s standard fee schedule and any modifications or revisions thereto. EAS may perform additional services at its discretion at EAS’s request for additional fees.

As standard practice, EAS sends a notification for the registration renewal of Clients product, as well as other services mutually agreed upon between EAS and the Client. However, it remains the Client’s responsibility to keep their registration current and active, either by contacting EAS for any such actions or directly by themselves.

EAS relies on email communication. All the important communication – including regulatory actions from the FDA, Registration renewal and other notifications – are notified through email. The primary communication language will be English. EAS may contact their Clients or the interested parties for the promotion of their services and updates on regulatory information. Users have the right to unsubscribe from the services, and EAS will act promptly on such requests.

In case of non-payment of any offered services, EAS has the right to revoke the services and will not be responsible for any losses or consequences caused by such a revocation of services.

EAS shall not be held responsible for breach of contract caused by an act of God, insurrection, civil war, military or local emergency, or by any act or failure to act by the U.S. Food and Drug Administration (FDA). Time shall not be of the essence for services to be rendered by EAS.

Client agrees to reimburse, indemnify, and hold harmless EAS from and against any and all expenses, costs, and claims, including claims by third parties, including but not limited to any governmental agencies, and related costs and attorneys' fees, and including but not limited to any fees owed to FDA, whether such claims are alleged in tort, contract, or under other law, arising out of or in connection with this agreement, the transactions contemplated hereby, any claim connected to the business or operations of Client, or any breach of law by Client. The client waives any and all claims against EAS arising out of or in connection with this agreement except for willful misconduct or gross negligence, and for those, EAS waives its claims to the extent the law permits.

EAS may terminate this agreement at any time upon giving written notice to Client by mail to the address stated above or provided by the client for its food facility registrations, or by electronic mail to the email provided by the Client.


Parties agree that EAS may utilize the services of a Third Party in the US to facilitate the FDA registration for the Client. Client agrees to reasonably cooperate with any such Third-Party providing services to Client on behalf of EAS.

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