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BioWorld - Sunday, April 5, 2026
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SEC: Cybersecurity incidents to be disclosed on 8-Ks

July 27, 2023
Public companies registered with the U.S. SEC will soon have to disclose material cybersecurity incidents and annually report material information regarding their cybersecurity risk management, strategy and governance.
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US FDA’s draft guidance for opioid use disorder devices greets tepid industry interest

July 27, 2023
By Mark McCarty
The U.S. FDA has issued a draft guidance for devices intended to address opioid use disorder (OUD), a problem with a massive public health footprint that has defied the efforts of public health programs. The draft guidance highlights some of the difficulties in executing pivotal studies for these devices, but the FDA’s July 27 press omits any mention of a 2018 innovation challenge for this category of devices, a programmatic effort that seems to have yielded little in the way of tangible results.
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Truvian's benchtop blood testing platform can deliver results similar to those generated by central laboratory

Truvian’s blood testing platform provides lab quality results

July 27, 2023
By Shani Alexander
News from Truvian Health Inc. that its benchtop blood testing platform can deliver results similar to those generated by central laboratory is promising for the diagnostic sector still coming to terms with fraudulent claims from companies such as Theranos Inc. and Arrayit Corp. that their various technologies were able to run an array of tests with just a few drops of blood.
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US Rx pricing pressure heats up for PBMs

July 27, 2023
By Mari Serebrov
Continuing its efforts to reduce prescription drug prices in the U.S., the Senate Finance Committee turned up the heat on pharmacy benefit managers (PBMs), voting overwhelmingly, 26-1, to send the bipartisan Modernizing and Ensuring PBM Accountability (MEPA) Act to the full Senate.
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FDA refuses to review NDA for Biohaven’s ultra-rare disease treatment

July 27, 2023
By Lee Landenberger
Not hitting the primary endpoint of a phase III study caused the U.S. FDA to say it would not review Biohaven Ltd.’s NDA for troriluzole to treat spinocerebellar ataxia (SCA), an ultra-rare disorder.
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SEC: Cybersecurity incidents to be disclosed on 8-Ks

July 26, 2023
Public companies registered with the U.S. SEC will soon have to disclose material cybersecurity incidents and annually report material information regarding their cybersecurity risk management, strategy and governance.
Read More
U.S. flag on columned building

US Senate focused on legislation and enforcement of vertical mergers

July 26, 2023
By Mark McCarty
The U.S. Federal Trade Commission (FTC) has been exceptionally active in the mergers and acquisitions space for the past 18 months, but Congress might soon amplify these agencies’ ability to suppress these transactions. Sen. Amy Klobuchar (D-Minn.), who chairs the competition subcommittee of the Senate Judiciary Committee, said in a recent hearing that vertical mergers have flown largely off the enforcement radar, a problem that Congress could address by several means, including by providing the FTC with a heftier budget to pursue these cases.
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U.S. Capitol building

Horizontal regulation of AI not ruled out in US Senate hearing

July 26, 2023
By Mark McCarty
The U.S. Senate held a July 25 hearing on the need for regulation of artificial intelligence (AI), which highlighted an interest in a single overarching agency that would direct any regulations promulgated for AI across the U.S. economy.
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US FTC finalizes endorsement, testimonial guides

July 26, 2023
By Mari Serebrov
Following a comment-and-review process waylaid by the COVID-19 pandemic, the U.S. FTC is finalizing its revised guides on the use of endorsements and testimonials in advertising.
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U.S. FDA approves Octapharma’s blood clotting treatment

July 26, 2023
The U.S. FDA has approved Balfaxar (prothrombin complex concentrate, human-lans) from Octapharma USA Inc.
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