The U.S. Food and Drug Administration (FDA) requires various types of registrations, depending on the nature of your business. Here are some common types of FDA registrations:

1. Food Facility Registration: If you manufacture, process, pack, or store food for consumption in the U.S., you need to register your facility with the FDA.
2. Medical Device Establishment Registration: Any establishment involved in the production and distribution of medical devices intended for use in the U.S. must register with the FDA.
3. Drug Establishment Registration: Manufacturers, repackers, and relabelers of drugs must register their establishments with the FDA.
4. Biologics Establishment Registration: Facilities involved in the manufacture of biological products must register with the FDA.
5. Cosmetic Registration: While not mandatory, the FDA encourages cosmetic companies to participate in the Voluntary Cosmetic Registration Program (VCRP).
6. Tobacco Product Establishment Registration: Domestic establishments engaged in manufacturing, preparing, compounding, or processing tobacco products must register with the FDA.

Steps to Register with the FDA

1. Determine the Type of Registration Required: Identify which type of registration applies to your business. Apply online with regpro.us
2. Create an FDA Industry Systems (FIS) Account: Our team will register for an account on the FDA’s Unified Registration and Listing System (FURLS).
3. Submit Registration Information: Our support team will login into your FIS account and submit the required information for your specific type of registration.
4. Pay Applicable Fees: Some registrations, like those for drug and medical device establishments, require payment of user fees.
5. Maintain and Update Registration: Our team will ensure your registration is renewed as required (usually annually) and update any changes to your business information.

If you have a specific type of product or facility in mind, contact us on support@regpro.us

To register with the U.S. Food and Drug Administration (FDA), the specific requirements and processes will vary depending on the type of business and the products or services you provide. Here is a general overview of the FDA registration process:

1. Determine Applicability: Identify whether your business or product falls under FDA regulation. The FDA oversees a wide range of products, including food, drugs (including prescription and over-the-counter medications), medical devices, dietary supplements, cosmetics, and more.

2. Obtain a DUNS Number: If your business is not already registered with the FDA, you will need to obtain a Unique number. This unique identifier and is required for certain FDA registrations.

3. Determine the Appropriate FDA Registration: Depending on your business and the products you deal with, you may need to register with specific FDA programs. For example:

   a. Food Facilities: If you are involved in food manufacturing, processing, packaging, or storing, you may need to register as a food facility with the FDA.

   b. Drug Establishments: If you manufacture, distribute, or package drugs (including over-the-counter medications), you may need to register as a drug establishment.

   c. Medical Devices: Manufacturers, distributors, and importers of medical devices are generally required to register their establishments and list their devices with the FDA.

   d. Dietary Supplements: If you manufacture or distribute dietary supplements, you may need to register with the FDA as a dietary supplement facility.

4. Complete the FDA Registration: Once you have determined the appropriate registration category, you will need to complete the registration process. This typically involves submitting an online application through the FDA’s registration portal, providing the necessary information about your business, products, and manufacturing processes.

5. Pay the Registration Fee: Depending on the specific FDA program and type of registration, there may be a fee associated with the registration process. Ensure you review the FDA’s fee schedule and make the necessary payment.

6. FDA Inspection (if applicable): Certain businesses may be subject to FDA inspections to verify compliance with regulatory requirements. This is more common for food facilities, drug establishments, and medical device manufacturers.

It’s important to note that the FDA registration process can be complex, and requirements can change over time. It is recommended to consult specialist and relevant guidance documents specific to your industry to ensure compliance with the most up-to-date regulations. Additionally, you may consider engaging with legal or regulatory experts familiar with FDA requirements to assist you with the registration process.