US FDA Registration is a mandatory requiremnet to place your products in USA. US FDA Registration is given under US bio-terrorism act. After registration you are allotaed  a registration number which is used bu US custom authority & other concerned authorities in USA to established your genuine identity as a suppliers to USA. US FDA registration is given in many categories. Most prominent categories are : US FDA Registration for Food, US FDA Registration for cosmetics, US FDA Registration for drugs, US FDA Registration for medical devices. Appart fro these US FDA Registration can also be obtained for packaging materials, utensils & some other product categories.

CDG is a regulatory compliance company specializing in the food, beverage, dietary supplement, alcoholic beverage, medical device and cosmetic industries. Our regulatory compliance specialists have decades of FDA industry and regulatory experience. Committed to maintaining our position as a leading provider of registration and listing services, we strategically focus our knowledge and limit our services. This approach assures that CDG always achieves the highest quality of service and continued client satisfaction.

The FDA requires all domestic and foreign facilities that manufacture, process, pack, or hold food, beverages or dietary supplements for importation or distribution in the United States to register with the FDA. Any imported foods or imported beverages not in compliance with FDA’s food facility registration requirements may be refused by FDA or CBP. Foreign food facilities must designate a U.S. Agent when registering their food facility with the FDA. The U.S. Agent is a person or entity located within, or that maintains an office, in the United States. The U.S. Agent plays the role of the domestic representative for the foreign facility through which all communication with the FDA takes place.Our top priority is providing outstanding customer service. We pride ourselves on responding promptly to clients’ needs and providing exceptional individual and business advice and services.

All commercial processors of low-acid and acidified foods located in the United States and all processors in other countries who export low-acid canned food or acidified food products into the United States must register their processing plants with FDA. Also, manufacturers must file documentation with FDA for each process used in the production of foods subject to these requirements. These submissions are known as a “Process Filing” and each is assigned a unique “Submission Identifier” (SID). Wholesalers, importers, distributors, brokers, etc. are not required to register and file processes. However, they must ensure that processing firms they represent comply with all registration and process filing requirements.

FDA Food & Dietary Supplement Labeling Requirements

​The US FDA has provided guidance for food & dietary supplement labeling Requirements. The guidance represents the FDA's thinking on the requirement. It does not create or confer any rights for or on any person and does not operate to bind FDA or the public. You can use an alternative approach if the approach satisfies the requirements of the applicable statutes and regulations. You can contact Willow Glen Consultancy staff to discuss more detail for labeling requirement. You can also contact the FDA staff responsible for implementing this guidance. 

CDG is a industry leader for 'US FDA Registration Services in India'. 'US Food Facility Registration' is our expertise though we do provide US FDA registration service in other product groups also. We mayl also service as authorised agent for US FDA. So if you have any query regarding US FDA Registration in India please contact us.

US FDA Registration is a mandatory requiremnet to place your products in USA. US FDA Registration is given under US bio-terrorism act. After registration you are allotaed  a registration number which is used bu US custom authority & other concerned authorities in USA to established your genuine identity as a suppliers to USA. US FDA registration is given in many categories. Most prominent categories are : US FDA Registration for Food, US FDA Registration for cosmetics, US FDA Registration for drugs, US FDA Registration for medical devices. Appart fro these US FDA Registration can also be obtained for packaging materials, utensils & some other product categories.

CDG is a regulatory compliance company specializing in the food, beverage, dietary supplement, alcoholic beverage, medical device and cosmetic industries. Our regulatory compliance specialists have decades of FDA industry and regulatory experience. Committed to maintaining our position as a leading provider of registration and listing services, we strategically focus our knowledge and limit our services. This approach assures that CDG always achieves the highest quality of service and continued client satisfaction.

The FDA requires all domestic and foreign facilities that manufacture, process, pack, or hold food, beverages or dietary supplements for importation or distribution in the United States to register with the FDA. Any imported foods or imported beverages not in compliance with FDA’s food facility registration requirements may be refused by FDA or CBP. Foreign food facilities must designate a U.S. Agent when registering their food facility with the FDA. The U.S. Agent is a person or entity located within, or that maintains an office, in the United States. The U.S. Agent plays the role of the domestic representative for the foreign facility through which all communication with the FDA takes place.Our top priority is providing outstanding customer service. We pride ourselves on responding promptly to clients’ needs and providing exceptional individual and business advice and services.

All commercial processors of low-acid and acidified foods located in the United States and all processors in other countries who export low-acid canned food or acidified food products into the United States must register their processing plants with FDA. Also, manufacturers must file documentation with FDA for each process used in the production of foods subject to these requirements. These submissions are known as a “Process Filing” and each is assigned a unique “Submission Identifier” (SID). Wholesalers, importers, distributors, brokers, etc. are not required to register and file processes. However, they must ensure that processing firms they represent comply with all registration and process filing requirements.

FDA Food & Dietary Supplement Labeling Requirements

​The US FDA has provided guidance for food & dietary supplement labeling Requirements. The guidance represents the FDA's thinking on the requirement. It does not create or confer any rights for or on any person and does not operate to bind FDA or the public. You can use an alternative approach if the approach satisfies the requirements of the applicable statutes and regulations. You can contact Willow Glen Consultancy staff to discuss more detail for labeling requirement. You can also contact the FDA staff responsible for implementing this guidance. 

CDG is a industry leader for 'US FDA Registration Services in India'. 'US Food Facility Registration' is our expertise though we do provide US FDA registration service in other product groups also. We mayl also service as authorised agent for US FDA. So if you have any query regarding US FDA Registration in India please contact us.