US FDA Registration In Hyderabad

CDG provides US FDA registration services in Hyderabad.

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, 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. 

The FDA's primary focus is enforcement of the Federal Food, Drug, and Cosmetic Act (FD&C), but the agency also enforces other laws, notably Section 361 of the Public Health Service Act, as well as associated regulations. Much of this regulatory-enforcement work is not directly related to food or drugs, but involves such things as regulating lasers, cellular phones, and condoms, as well as control of disease in contexts varying from household pets to human sperm donated for use in assisted reproduction. 

In the past 10 years, we have developed experience and understanding of the knowledge and skills needed to address a wide variety of regulatory issues. This means that we can offer solutions that add value, saving you both money and time. We believe in a transparent approach to business, and always put our customers at the center of our work. We strive to achieve excellent customer satisfaction through superior services. 

CDG offer the lowest guaranteed fees for quality services. Our charges are disclosed upfront, and there are no hidden costs or increased annual fees.