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ND Regulators Approve Bank-to-Bank Stablecoin Use North Dakota’s Industrial Commission approved the use of the state bank’s planned stablecoin, the Roughrider Coin, for bank-to-bank transactions...
Tech Group Pushing Back on NY Chatbot Bill A tech industry group is opposing a New York bill ( SB 7263 ) aimed at preventing chatbots from impersonating a variety of licensed professionals, including...
KS Lawmakers Pass PBM Bill A bill aimed at tightening regulations on PBMs ( SB 360 ), but which appeared unlikely to move forward this session, was inserted into another bill ( SB 20 ) during a conference...
Who could have predicted this? Prediction markets have emerged as one of the biggest stories of 2026. The online platforms and apps, which allow users to bet on anything from who will win the Oscar for...
New White House Policy Framework Calls for Blocking State AI Laws The Trump administration released a National Policy Framework for Artificial Intelligence that, among other things, urges Congress to...
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Virginia lawmakers have passed legislation (SB 271/HB 483) that would create a prescription drug affordability board to review drug prices and set limits on how much state-regulated health plans can pay for drugs. The legislation is similar to that enacted in other states, but Virginia’s would be the first linking the board’s activity to drug price negotiations between manufacturers and Medicare mandated by the federal Inflation Reduction Act of 2022. (PLURIBUS NEWS, LEXISNEXIS STATE NET)
After decades of debating whether to restrict direct-to-consumer drug advertising, the Trump administration and federal lawmakers appear to be moving in that direction.
Last February, U.S. Sen. Angus King (I-ME) introduced a bill (SB 483) prohibiting drugs from being advertised directly to consumers for three years after they receive FDA approval. The measure is still pending.
In September President Trump issued a presidential memorandum calling for the reversal of a 1997 policy change that allowed drug advertising on television. On the same day, the FDA announced that it was “sending thousands of letters warning pharmaceutical companies to remove misleading ads and issuing approximately 100 cease-and-desist letters to companies with deceptive ads.” (NEW YORK TIMES)
—Compiled by SNCJ Managing Editor KOREY CLARK
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