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 The Voluntary Qualified Importer Program (VQIP) 

For participants in the Voluntary Qualified Importer Program (VQIP) under the FDA Food Safety Modernization Act (FSMA), the 2025/2026 benefit year started October 1, 2025, and ends September 30, 2026.  

VQIP is a voluntary, fee-based program that provides importers who achieve and maintain control over the safety and security of their supply chains, expedited review and importation of human and animal foods into the United States. 

VQIP participants can import certain food products into the United States with quicker, easier entry, limited examination and sampling, FDA sampling at preferred location, and faster lab results with the assistance of the VQIP Importers Help Desk. 

To participate in VQIP, food importers must meet certain eligibility requirements, including ensuring that the facilities of their foreign suppliers are certified through the FDA’s Accredited Third-Party Certification Program. Importers interested in participating must apply using the VQIP application portal. The portal will reopen on January 1, 2026, and remain open through September 1, 2026, for the 2026/27 program. 

To see a current list of VQIP participants, visit: Public List of Approved VQIP Importers 

The following resources provide more in-depth information about the VQIP program and process: 

VQIP supports the FDA Strategy for the Safety of Imported Food by incentivizing importers to use certified suppliers and maintain robust processes and procedures to help ensure imported food is meeting U.S. food safety requirements 

Those interested should submit questions to the VQIP Importers Help Desk by email FSMAVQIP@fda.hhs.gov or by phone 301-796-8745. 

Learn more about Importing Food Products into the United States.

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★★★★★

Working with Shelly on various new product launches over the last couple of years has been seamless. Quick and clear guidance is always what we get.
R.G. Client
I've been working with Shelly and her team at Garg law for a little while now and they are fantastic! Very responsive, professional and they certainly get things done. Extremely satisfied with their service and highly recommend.
Mike H. Client
Ms Garg helped my company navigate an FDA import issue. She achieved an excellent result, was very responsive and professional, and managed to keep the project within budget. She is a stellar attorney.
Dr. Sastry Client
I have been using Shelly Garg as FDA Counsel for 10+ years, since she was at another international law firm. While we continued to use the previous firm she was at (mainly due to the process required to change firms), we realized the quality of counsel was not the same. We have since been using Garg Law and the ease of use and trust in the knowledge was back instantly. Shelly has the skills to help me understand the regulations (by translating into layman's terms) and risks in a manner that is specific to my business. She is also extremely timely in her responses which is critical when we have a deadline mandated by the FDA. Many other attorneys cite the regulations which l've already read, but need further counsel. In my opinion, this demonstrates Shelly's in-depth knowledge of the regulations, how they pertain to the law, and how they are applicable IRL. Shelly's personable approach and pleasant manner in communication makes it very easy to have been work with her and have productive discussions on the best next steps. She truly has a passion iternational for all things FDA and I've learned so much from her.
Claire P. Client

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