Fda Maharashtra Manufacturer Login

All Drug MFG Licensee are informed to Register themselves and Upload Documents / informations for Making Online submission of data through Sugam Portal as per mandatory requirement under the Rule 84AB vide notification GSR 19E Dated:10-01-2019

All the registered users holding valid WHO-GMP certificate are hereby instructed to update their information such as manufacturing license details/ copies, product permission, WHO-GMP certificate & its validity details of products approval/COPPs granted under current certification, contact details and contact person details.

All the registered users holding valid WHO-GMP certificate are hereby instructed to update their information such as manufacturing license details/ copies, product permission, WHO-GMP certificate & its validity details of products approval/COPPs granted under current certification, contact details and contact person details.

All the registered users holding valid WHO-GMP certificate are hereby instructed to update their information such as manufacturing license details/ copies, product permission, WHO-GMP certificate & its validity details of products approval/COPPs granted under current certification, contact details and contact person details.

All the registered users holding valid WHO-GMP certificate are hereby instructed to update their information such as manufacturing license details/ copies, product permission, WHO-GMP certificate & its validity details of products approval/COPPs granted under current certification, contact details and contact person details.

Food and Drug Administration Maharashtra State is the State prime organization of consumer protection. It has dedicated professionals working to protect, promote and enhance the health of people. It is a trusted agency to enforce the Food Safety & Standards Act 2006, Drug and Cosmetics Act fairly, upholds safety standards, and protects consumers.

Before using FDA's Direct system, FDA strongly encourages you to have current antivirus and antispyware software installed on your computer to help ensure the privacy of the information being entered. Browser Compatibility: The CDER Direct portal currently works best with the following browsers: Microsoft Internet Explorer 8 (IE8) and above

FDA Industry Systems (FIS) was created to facilitate making submissions to the U.S. Food and Drug Administration (FDA), including registrations, listings, and other notifications. FIS has been available 24 hours a day, seven days a week, since October 16, 2003 6:00 p.m. EDT. FIS was created, in part, in response to the Bioterrorism Act of 2002 ...