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FDA Updates Guidance for the Voluntary Qualified Importer Program (VQIP)

The U.S. Food and Drug Administration (FDA) today released guidance with revisions to the FDA Food Safety Modernization Act (FSMA) Voluntary Qualified Importer Program (VQIP). VQIP offers importers who achieve and maintain a high level of control over the safety and security of their supply chains expedited review and importation of human and animal foods into the United States. These updates are intended to streamline processes, enhance flexibility, and elevate the overall efficiency of the program.

Through the updates made today, the FDA is implementing a revised inspection approach, strategically designed to optimize program efficiency by leveraging other oversight activities, which may reduce user fees. 

Additionally, participants now have the flexibility to add new foreign suppliers and foods to their existing program throughout the fiscal year, allowing them to access more benefits through their program. To support our participants in obtaining a facility certificate from an accredited certification body under the Accredited Third-Party Certification Program (TPP), we are also extending the deadline for submitting the notice of intent to participate and application. 

Expedited entry through VQIP incentivizes importers to adopt a robust system of supply chain management and further benefits public health by allowing FDA to focus its resources on food entries that pose a higher risk to public health. These updates, which are effective immediately, build on feedback from stakeholders to support and streamline the process for participation. 

All interested food importers can take advantage of the benefits of VQIP, which can include:

  • Streamlined importation processes, saving food importers valuable time and resources;
  • Avoiding unexpected delays at the point of import;
  • Reduced storage costs, enabling food importers to optimize their resources efficiently; and
  • Recognition as a responsible importer committed to food safety and security.

To learn more about VQIP contact fsmavqip@fda.hhs.gov.

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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.
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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.
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