August 28, 2025: Washington, DC – The National Consumers League (NCL) is greatly concerned about the recent upheaval at the Centers for Disease Control and Prevention (CDC), including the abrupt ousting of CDC Director Susan Monarez less than a month after she was sworn in.
August 11, 2025: Washington, DC – The National Consumers League (NCL) won an important legal victory this week in its case against Starbucks when a Superior Court judge in the District of Columbia rejected the company’s motion to dismiss a lawsuit brought by NCL.
August 4, 2025: Artificial intelligence is not on the way; it’s already here. It’s recommending your next playlist, filtering your job applications, deciding what shows up on your feed, and even answering your Google search. As AI gets smarter, faster, and more prominent in our lives, it raises the question: What is protecting my generation, Generation Z, from AI?
July 28, 2025: Following the growth of online sports betting and increased data documenting associated harms, NCL has released its first report on sports betting companies’ advertising practices. The report focuses on sports betting apps and how they use smartphone notifications to advertise to consumers. After concluding its study, NCL believes that sports betting companies’ use of push notifications for marketing purposes may violate federal law as a prohibited unfair practice. The full report is available here.
July 28, 2025: In a first-of-its-kind report, NCL has found that 93% of smartphone notifications sent by the three biggest sports betting companies during a 4-week period contained advertising material. The findings are based on the collection of more than 100 notifications. To stop the flood of marketing, NCL is advocating for a prohibition on sports betting advertising, especially the use of push notifications for this purpose. NCL is not advocating for a ban on sports betting.
July 23, 2025: Washington, DC – The Supreme Court of the United States, in a 6-3 decision, has upheld the President’s dismissal of three Democratic Commissioners of the Consumer Product Safety Commission (CPSC) as the broader merits of the firing are being adjudicated in the courts.
July 23, 2025: Washington, DC – The National Consumers League (NCL) is proud to announce the winners of the 2025 Script Your Future Team Challenge, an annual competition that engages pharmacy students in raising awareness about the importance of medication adherence.
July 22, 2025: Washington, DC— The National Consumers League, Consumer Federation of America, and Consumer Reports led a letter signed by 100 stakeholders calling on President Trump to rescind the unlawful attempted removal of the Democratic Commissioners at the Consumer Product Safety Commission (CPSC). On May 8th, the Trump administration attempted to illegally fire Commissioners Alexander Hoehn-Saric, Richard Trumka, and Mary T. Boyle, who were later reinstated by court order.
July 21, 2025: Washington, DC– Today, the National Consumers League, Consumer Federation of America, Consumer Reports, and 118 other stakeholders sent a letter to congressional leaders calling on Congress to preserve an independent, bipartisan Consumer Product Safety Commission (CPSC) and ensure the agency has the appropriate tools, resources, and personnel to carry out its lifesaving mission.
July 18, 2025: Washington, DC – The National Consumers League (NCL) and 17 other safety organizations today sent a letter to the House Appropriations Committee calling on Congress to provide the National Highway Traffic Safety Administration (NHTSA) with the resources necessary to reduce the unacceptably high number of deaths and injuries caused by traffic crashes.
The work of the National Consumers League is making a difference in people’s lives across the country. Meet some of the consumers touched by our programs.
Read about NCL’s impact
Paige, 55, a Nashville wife and mother of two, answered an employment ad for secret shoppers. Before sending payment to the scammers, she reached out to NCL.
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A grease fire flared up in Decklan’s kitchen. As his family scrambled and panicked, fearing that the whole house might erupt in flames, Decklan remained calm. He hurried over to the pantry, grabbed some baking soda, and dumped it on the fire quickly extinguishing the blaze.
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Cincinnati resident Charles, 45, lost his computer business — and health insurance— during a time of economic downturn. A diabetic, Charles was now unable to afford his medication. He stopped taking it which made him seriously ill and put his life at risk.
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Jeremy is a fast-food worker who has been employed at a number of Chipotle restaurants in New York City. When he was just 20 years old, he took part in an NCL research project that revealed that management practices within the fast food chain were putting workers—and food safety for customers—at risk.
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By Sally Greenberg, NCL Executive Director
While the COVID-19 pandemic has led to hardship for all Americans, it is clear that people of color have been disproportionately burdened. Across the health care continuum, addressing this disparity has become part of the broader conversation about the history of systemic racism and the underlying social determinants of health that negatively affect the mental, physical, and economic health of individuals and entire communities.
The pandemic has underscored persistent health disparities, and there is growing recognition that representation in research and clinical trials can have a profound impact on health outcomes. A lack of representation from racially and ethnically diverse groups in research and clinical trials have typically led to gaps in data, missing the opportunity to assess the full impact of various treatments and drugs across a range of populations. The collection and use of real-world research and data to inform the potential use, risks, and benefits of medical products and treatments can ultimately lead to better health outcomes, particularly for those who have been underrepresented in the past.
Existing efforts to improve inclusion
Efforts to expand diversity and representation in medical research are underway in Congress. Policymakers are encouraging the incorporation of Real World Evidence (RWE) in drug development through the recent Cures 2.0 draft legislation released by Reps. Diana Degette (D-CO-1) and Fred Upton (D-MI-6). While the status quo limits us from effectively reaching underserved populations, the proposed legislation would allow studies that include RWE for some drugs after they have been approved. At the heart of this issue is a growing appreciation that the same therapy can affect different populations in different ways, which is why Cures 2.0 supports collecting data that more accurately reflects the unique experiences and needs of patients across diverse populations.
Recognizing the potential for RWE in maternal health
The lack of representative research in the field of maternal health is undeniable, and its implications are staggering. The dismal state of maternal care in the United States reflects how our health care system has failed women of color, including by not adequately studying treatment options to prevent maternal morbidity and mortality. The need for RWE is clear when you consider the persistent disparities in health outcomes that plague minority communities.
Preterm birth and its disproportionate impact on women of color is a stark illustration of the need to make progress on representative research in maternal health. Preterm birth is the second-largest contributor to infant death in America today. Despite the tremendous physical, emotional, and financial toll that preterm birth continues to take on our country — disproportionately so on women and families of color — not enough therapeutic tools currently exist to prevent it.
Today, “17P,” the only FDA-approved treatment to help reduce the likelihood of spontaneous, recurrent preterm birth in the United States is at-risk of being withdrawn from the market in all its forms, including the branded product and five generic versions. Unfortunately there is conflicting evidence from two different clinical trials, one representative of a diverse U.S. population and another studied in a largely white population in Europe. It’s not a straightforward comparison. If 17P is withdrawn, the women most affected by preterm birth, predominantly women of color, would be left without an FDA-approved treatment option.
The FDA is considering the path forward, including additional data collection through leveraging RWE from past patient use. The success of the first (approval) trial for 17P in the impacted communities signals the importance of RWE. Continued access to 17P is, at its core, a matter of health equity. Black women must not yet again be left vulnerable to a system that historically has overlooked them.
