CDG provides US FDA registration services in Ahmedabad.CDG is a leading organization in US FDA Registration in India.

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. 

If you want to export products in the USA, you need to comply with certain US Import and Export Formalities. One such mandatory requirement you need to fulfill is US FDA Certification. It is a basic requirement that you need to export products such as Food, Drugs, Cosmetics, Color Additives, Medical Devices, supplements, and even PPE Kit. Thus, it is important to get a US FDA certificate in India for every exporter exporting these products to the USA. In this article, you will get to know the complete process to get a US FDA Certificate in India. 

What is the US FDA certificate in India? 

FDA (Food and Drug Administration) is a US Government Agency. It was established under the Federal Food and Drugs Act. 

The basic purpose of the US FDA is to protect and manage public health. Furthermore, the FDA works as a regulatory body. So, it ensures public safety by regulating the manufacturing, marketing, and distribution of a variety of products. 

Complete process to get US FDA Certificate in India 

The FDA has the power to investigate other nations’ facilities that export food and pharmaceutical items to the US. Food and pharmaceutical facilities operating in India that export goods to the U.S. need to mandatorily follow the FDA’s Current Good Manufacturing practices requirements (CGMP) in order to get US FDA Certificate in India. The complete process to get US FDA Certificate in India is as follows: 

Easy and Free Consultation with our US FDA Certification Experts for understanding the requirements, eligibility criteria, and document preparation. 

Choose a Package and Online Submission of the required documents on our web portal. 

Our team will designate a US FDA Agent who is registered in the United States and then submit the application to the US Food and Drug Administration. 

FDA Officials visit your manufacturing plant in India 

After the FDA Department and US FDA Officials successfully inspect your business and get satisfactory verification, they will approve the import of the drug or any other product and we will deliver your US FDA Certification in India through your preferred online channel. 

The United States Food and Drug Administration (FDA or USFDA) is a federal agency of the Department of Health and Human Services. The FDA is responsible for protecting and promoting public health through the control and supervision of food safety, products, dietary supplements, prescription and over-the-counter pharmaceutical drugs (medications), vaccines, biopharmaceuticals, blood transfusions, medical devices, electromagnetic radiation emitting devices (ERED), cosmetics, animal foods & feed and veterinary products. 

CDG provides US FDA registration services in Ahmedabad.CDG is a leading organization in US FDA Registration in India.

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. 

If you want to export products in the USA, you need to comply with certain US Import and Export Formalities. One such mandatory requirement you need to fulfill is US FDA Certification. It is a basic requirement that you need to export products such as Food, Drugs, Cosmetics, Color Additives, Medical Devices, supplements, and even PPE Kit. Thus, it is important to get a US FDA certificate in India for every exporter exporting these products to the USA. In this article, you will get to know the complete process to get a US FDA Certificate in India. 

What is the US FDA certificate in India? 

FDA (Food and Drug Administration) is a US Government Agency. It was established under the Federal Food and Drugs Act. 

The basic purpose of the US FDA is to protect and manage public health. Furthermore, the FDA works as a regulatory body. So, it ensures public safety by regulating the manufacturing, marketing, and distribution of a variety of products. 

Complete process to get US FDA Certificate in India 

The FDA has the power to investigate other nations’ facilities that export food and pharmaceutical items to the US. Food and pharmaceutical facilities operating in India that export goods to the U.S. need to mandatorily follow the FDA’s Current Good Manufacturing practices requirements (CGMP) in order to get US FDA Certificate in India. The complete process to get US FDA Certificate in India is as follows: 

Easy and Free Consultation with our US FDA Certification Experts for understanding the requirements, eligibility criteria, and document preparation. 

Choose a Package and Online Submission of the required documents on our web portal. 

Our team will designate a US FDA Agent who is registered in the United States and then submit the application to the US Food and Drug Administration. 

FDA Officials visit your manufacturing plant in India 

After the FDA Department and US FDA Officials successfully inspect your business and get satisfactory verification, they will approve the import of the drug or any other product and we will deliver your US FDA Certification in India through your preferred online channel. 

The United States Food and Drug Administration (FDA or USFDA) is a federal agency of the Department of Health and Human Services. The FDA is responsible for protecting and promoting public health through the control and supervision of food safety, products, dietary supplements, prescription and over-the-counter pharmaceutical drugs (medications), vaccines, biopharmaceuticals, blood transfusions, medical devices, electromagnetic radiation emitting devices (ERED), cosmetics, animal foods & feed and veterinary products.