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Text Content

Ph: +1(630) 270-2921
Email: info@fdahelp.us
 * 
 * Register with FDA

 * Home
 * Drugs
   * Compounding Pharmacy Registration
   * OTC Drug Products
   * NDC Number
   * Drug Master Files
   * Drug Establishment Registration
   * Drug Registration Renewal
   * Drug Reporting
 * Medical Devices
   * Premarket Notification (510k)
   * Establishment Registration and Listing
   * Medical Device Registration Renewal
   * Medical Device Labeling
   * UDI submission
   * CE Marking
 * Cosmetics
   * FDA Cosmetic Registration - MoCRA
   * Cosmetic Registration
   * Cosmetics Labeling Review
   * EU Cosmetic Regulations
 * Food
   * Registration of Food Facilities
   * Acidified & Low-Acid Canned Foods
   * Dietary supplement
   * Prior notice
   * Food Contact Substances
 * Fees
 * Forms
   * Registration Forms
      * Medical Device Registration
      * Food Facility Registration
      * Drug Registration
      * Drug Listing
      * Prior Notice
      * Self Identification
      * UDI Registration - Part1
      * Cosmetic Facility Registration
      * Cosmetic Product Listing
     
     Label Review Forms
      * Medical Device Label Review
      * Food Label Review
      * Drug Label Review
      * Cosmetic Label Review
 * Contact us

MENU
 * 
 * 








FDA REGISTRATION - FDA CERTIFICATE - FDA AGENT


FDA REGISTRATION



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 CERTIFICATION



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 CERTIFICATE



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.

ABOUT US



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 Food Facility Registration
 * Dietary Supplement Registration
 * FDA Registration Certificate
 * U.S. FDA Agent Requirements
 * FDA Agent Services
 * Food Registration - FAQ
 * FDA Registration & US Agent Fees
 * FDA registration and labeler code
 * Hand Sanitizer Regulations - US FDA

 * OTC Drug Establishment Registration
 * Drug Establishment Registration
 * Compounding pharmacy registration
 * NDC Labeler code
 * NDC Labeler Code Assignment
 * OTC-Monograph
 * Homeopathic Registration
 * API Drug Registration
 * Hand Sanitizer - FDA final rule

▼

VERIFY CERTIFICATE

Certificate Number:




FDA REGISTRATION FORMS

 * Food Facility Registration Form
 * Medical Device Registration Form
 * NDC Labeler Code Request Form
 * Drug Registration Form
 * Drug Listing Form
 * Prior Notice Form
 * Cosmetic Facility Registration Form

POPULAR PAGES

 * 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 2024

CONTACT US

LIBERTY MANAGEMENT GROUP LTD.

75 Executive Drive, Suite 114
Aurora, Illinois, USA - 60504
Food : +1 (331) 465-4972
Drug : +1 (331) 218-8946
Cosmetics : +1 (630) 864-9023
Medical Device : +1 (331) 218-8946
Other : +1 (630) 270-2921
E-mail : info@fdahelp.us



EXPERIENCE OUR EXPERTISE:
VIEW OUR 510(K) PORTFOLIO



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Home | Drugs | Medical Devices | Cosmetics | Food | Associates | Newsletter |
Website Policy | Site Map | Contact us

Copyright © LMG ltd All rights reserved.

 * 
 * 
 * 
 * 


REGISTER WITH FDA

Please select the type of registration:

 * Food / Supplement Registration
 * Medical Device Registration
 * Drug Registration
 * NDC Labeler Code

 * Drug Listing
 * Cosmetic Facility Registration
 * Cosmetic Product Listing
 * Prior Notice


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