CDG Provides US FDA registration in Pune.

The U.S. Food and Drug Administration (US FDA) is responsible for assuring that food sold in the United States is safe, wholesome and properly labeled. This applies to food produced domestically, as well as food from foreign countries. The Federal Food, Drug, and Cosmetic Act (FD and C Act) and the Fair Packaging and Labeling Act are the Federal laws governing food products under US FDA jurisdiction. 

US FDA Certificate 

The US FDA Certificate generally means that companies registered with the US food and drug administration are often asked by their customers and suppliers to verify their registration number and registration validity date especially in the case of food manufacturers & exporters 

Manufacturers, Exporters, and Traders across the globe are curious to have the word “FDA Certified” in the name of the company. But this is not possible!  The FDA will not issue any kind of certificate to any organization other than domestic manufacturing companies. 

US FDA Certificate for Export 

Domestic firms exporting products from the United States are often asked by their foreign customers or foreign governments to supply an “FDA certification” for products regulated by the food and drug administration. A US FDA Certificate is a document prepared by the U.S. Food and Drug Administration, containing information about a product’s regulatory or marketing status. 

We are US FDA agents and regulatory consultants having offices in the USA, Germany, and India. 

We issue certificate which serves as a third-party confirmation of your registration status. 

The third-party FDA Certification will not have any legal validity, nor does the US FDA recognizes this certificate of registration issued. 

FDA Registration 

FDA registration is the basic requirement for domestic and foreign establishments that manufacture or market food, drug, API, or medical device in the USA. FDA registration is not mandatory for cosmetic establishments, but they can participate in FDA voluntary cosmetic registration program (VCRP). 

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. 

CDG Provides US FDA registration in Pune.

The U.S. Food and Drug Administration (US FDA) is responsible for assuring that food sold in the United States is safe, wholesome and properly labeled. This applies to food produced domestically, as well as food from foreign countries. The Federal Food, Drug, and Cosmetic Act (FD and C Act) and the Fair Packaging and Labeling Act are the Federal laws governing food products under US FDA jurisdiction. 

US FDA Certificate 

The US FDA Certificate generally means that companies registered with the US food and drug administration are often asked by their customers and suppliers to verify their registration number and registration validity date especially in the case of food manufacturers & exporters 

Manufacturers, Exporters, and Traders across the globe are curious to have the word “FDA Certified” in the name of the company. But this is not possible!  The FDA will not issue any kind of certificate to any organization other than domestic manufacturing companies. 

US FDA Certificate for Export 

Domestic firms exporting products from the United States are often asked by their foreign customers or foreign governments to supply an “FDA certification” for products regulated by the food and drug administration. A US FDA Certificate is a document prepared by the U.S. Food and Drug Administration, containing information about a product’s regulatory or marketing status. 

We are US FDA agents and regulatory consultants having offices in the USA, Germany, and India. 

We issue certificate which serves as a third-party confirmation of your registration status. 

The third-party FDA Certification will not have any legal validity, nor does the US FDA recognizes this certificate of registration issued. 

FDA Registration 

FDA registration is the basic requirement for domestic and foreign establishments that manufacture or market food, drug, API, or medical device in the USA. FDA registration is not mandatory for cosmetic establishments, but they can participate in FDA voluntary cosmetic registration program (VCRP). 

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.