FDA Registration - FDA Certificate - FDA Agent
FDA registration is the basic requirement for domestic and foreign establishments that manufacture or market food, drug, API, medical devices, or cosmetic products in the USA. Companies that manufacture, process, pack, or store these products in the United States may be required to register with the FDA. Here are some examples of the types of companies that require FDA registration:
- Food manufacturers, processors, and packers
- Drug manufacturers, packers, and repackers
- Medical device manufacturers and importers
- Cosmetics manufacturers and processors
It's important to note that the FDA has specific registration requirements for each type of product, and the registration requirements for all kinds of companies are not the same.
US FDA Agent
All foreign Establishments must identify a US FDA Agent while in the registration process. This is a mandatory requirement, and without US FDA Agent, the registration cannot be completed. Liberty Management Group Ltd provides US FDA Agent service to foreign food, drug, API, and medical device establishments.
FDA Registration Renewal
All Drug, API, and Medical Device establishments registered with FDA must renew their registration annually between October 1st and December 31st. Food facilities must renew their FDA registration between October 1st and December 31st of every even-numbered year (once every 2 years). The FDA may consider the products of companies that do not comply with FDA renewal requirements as misbranded and may lead to FDA detention of your products.
FDA Registration or FDA registration number does not denote FDA certification or FDA approval of your facility or products. Any representation of the FDA registration number on the product label or labeling which implies FDA certification or FDA approval of a facility or product is misleading and may cause misbranding of the product.
FDA will not issue a registration certificate after completing the registration; also, FDA will not recognize a third-party registration certificate. Most Importers and Shipping companies always ask for an FDA registration certificate or proof of FDA registration from the manufacturer. LMG will issue a certificate of FDA registration to our clients for their records free of cost. Our clients and their customers can verify the certificate on our website.
FDA Registration Fees
Liberty Management Group LTD offers the most competitive fees for FDA registration, US FDA agent service, NDC number request, Drug listing, Label review, and other services. All our prices are published on the LMG website, which will help you calculate the total cost involved before starting the project.
Liberty Management Group Ltd is a globally recognized FDA, CE Marking, and ISO consulting firm headquartered in Illinois, USA, with Associates and offices around the globe. At LMG, we provide a full range of consulting services to domestic and foreign establishments in FDA regulations.
If you are looking for assistance in FDA regulations, FDA registration, or US FDA Agent requirements, LMG will be the best choice. Our dedicated and experienced consultants can provide exceptional guidance on US FDA regulations. We always give you an accurate estimate of the total cost involved in each project; we will never put you in uncertainty with hourly consulting fees. LMG provides quality service at a reasonable price within a minimum time frame.
Our mission is to provide maximum benefits to our clients through the proper guidance in FDA regulations and provide the latest information about the changes in FDA regulations.Quick links
- FDA Registration Number Search
- FDA Registration Renewal
- FDA Drug Registration Renewal
- FDA Drug Listing Renewal
- FDA Medical Device Renewal
- How to Register with FDA
- How to get FDA Approval
- How to get FDA Certification
- How to get ISO Certification
- DUNS Number Requirements - FAQ
- FDA UFI For Food Facility Registrations
- FDA Medical Device Fees - 2024
- FDA OTC Drug Facility Registration Fees 2023
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