Contact us

Thank you for your interest in Garg Law PLLC.

Our commitment to understanding your regulatory questions and business goals, and helping you achieve results starts here.

If you are looking for representation on a new matter, please fill out the form below to request a free consultation. The form enables us to conduct a preliminary check for potential conflicts of interest and to determine if we can proceed with the free consultation.

FDA Announces Release of Long-Term National Strategy to Increase the Resiliency of the U.S. Infant Formula Market

US Infant Formula Market

Today, the U.S. Food and Drug Administration (FDA) released a Long-Term National Strategy to Increase the Resiliency of the U.S. Infant Formula Market. The strategy builds on the Immediate National Strategy to Increase the Resiliency of the U.S. Infant Formula MarketExternal Link Disclaimer which was released in early 2023 in direct response to the February 2022 infant formula recall and the subsequent shortage of infant formula in the U.S. The long-term strategy identifies the actions we have taken since 2023 and focuses on our long-term goal of achieving a more robust and nimble U.S. infant formula supply.

In March 2023, the FDA released an Immediate National Strategy to Increase the Resiliency of the U.S. Infant Formula Market, which collected observations, described immediate actions, and detailed short-term plans to improve the resiliency of the U.S. infant formula supply. Simultaneously, the FDA partnered with the National Academies of Sciences, Engineering and Medicine (NASEM), as directed by Congress, to further study challenges to the infant formula market in the U.S. in order to inform a long-term strategy. 

In July 2024, NASEM produced a report titled Challenges in Supply, Market Competition, and Regulation of Infant Formula in the United StatesExternal Link Disclaimer, which further emphasized the need for a multi-faceted approach to building resiliency into this important industry. The important lessons learned from both the immediate strategy and the NASEM report, as well as valuable insights from industry, healthcare professionals, consumer groups, regulatory partners, and other stakeholders on this issue have culminated in the development of this Long-Term National Strategy to Increase the Resiliency of the U.S. Infant Formula Market.

In the long-term strategy, we outline long-term actions to improve information-sharing across all stakeholder groups, as well as actions taken since 2023, to help protect the integrity of the infant formula supply chain. The long-term strategy also addresses implementing measures for preventing contamination, incentivizing new infant formula manufacturers to enter the U.S. market, as well as authorities needed to gain better insight into the supply chain and risk for shortages. Through this strategy, we aim to focus efforts on the areas where we have seen the largest impact, illustrate the accomplishments we have achieved in protecting this vital source of nutrition for our most vulnerable population, and highlight where more efforts are needed to continually improve the supply for years to come. The FDA is committed to working with all stakeholders to improve the resiliency of the infant formula supply and to ensure that consumers have the utmost confidence that the infant formula available in the U.S. is safe and nutritious.

Additional Resources

Request a Consultation

★★★★★

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

News & Insights

Get the latest news on FDA regulatory delivered straight to your inbox.