With RFK Jr. Responsible, supplement manufacturers see the chance to collect

Last autumn, before being called US high official, Robert F. Kennedy Jr. said that the Trump administration will free Americans from “aggressive suppression” of vitamins, dietary supplements and other substances – the conclusion of the “Agency’s War Federal against the public health ”, as he said.

In fact, the FDA cannot even require supplements to be effective before being sold. When the Congress, at the request of the Agency, took into account the last legislation requesting vitamin producers, herbal remedies and other pills and potions to demonstrate the proof of their safety and value before marketing the products, it has received several E -negatives, Telephone calls and telegrams than at any time from the Vietnam War, through some accounts. The realization led to a 1994 law that allowed the food supplements industry to put its products on the market without testing and to get unproceated benefits, as long as appreciation does not include claims to treat or cure a disease. Industry annual revenues have increased from $ 4 billion to $ 70 billion since then.

With Kennedy now on the driver’s seat, the industry will probably expect more: it aims to make bold health requests for its products and even get the government, private insurers and flexible expense accounts to pay supplements, putting it in essence. on a stage of equality with pharmaceuticals approved by FDA.

On February 13, on the day Kennedy was cursed as a secretary of human health and services, President Donald Trump issued a “Do healthy America again” The agenda that concerns the alleged corruption of health regulation agencies and their training to “ensure the availability of extended treatment options and flexibility to cover health insurance to provide benefits that support the beneficial changes in lifestyle and disease prevention.”

Kennedy said exercises, dietary supplements and nutrition, rather than pharmaceuticals, are essential for good health. Supplements manufacturers want consumers to be able to use programs such as health, medicine and even benefit from the additional nutrition or SNAP assistance program, to pay items such as vitamins, fish oil, protein powders and probiotics.

“In essence, they are looking for a government subsidy,” said Pieter Cohen, a doctor of Harvard University who is studying supplements.

While the Senate Finance Committee has questioned Kennedy during its confirmation session on January 29, the natural health alliance supporters were lured on the quinoa salad in the US Capitol Center and it was crammed that the moment A finally arrived for their Movement of freedom of healthwhich has combined freedom capitalism and distrust in medical unity to champion irregular compounds since the 19th century.

“The biggest opportunity for our lives is before us,” said Jonathan Emord, the general counselor of the group, who has introduced many successful processes against FDA restrictions on unprobed health claims. “RFK has dedicated the whole life to oppose the unjustified influence” of the pharmaceutical industry and “ensuring that our triumph interests,” Emord said.

In speeches and in a pamphlet called “Maha mandate”, Emord and the founder of the Alliance, Robert Verkerk, said Kennedy will release companies to make higher claims for the alleged benefits of their products. Emord said that his group is preparing to sue the FDA to prevent the restriction of non-pharmaceutical production of substances such as biopeptides-complex molecules related to drugs such as Ozempic.

HHS spokesman Andrew Nixon did not respond to a comment request regarding the agency’s plans for food supplements.

While the basic law regulating the FDA establishes that a substance that is supposed to have curative treatment or effects is, by definition, a “drug” and, therefore, enters into the requirements of the Agency for High Standards of Scientific Evidence, the new Administration could reallocate the money away from execution, said Mitch Zeller, the former head of the FDA center for tobacco products.

As a Senate assistant at the beginning of his career, Zeller investigated an affected L-Triptophan supplement that killed at least 30 people and became thousands in the US in 1989. The scandal caused the FDA to seek a harder regulation of supplements, But a strong reaction resulted in the relatively weak law of supplements since 1994.

Even the application of the law could be decreased with a stroke stroke that would keep FDA inspectors outside the ground, Zeller said.