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BioWorld - Sunday, April 26, 2026
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FDA trial oversight lacking, new analysis says

Oct. 1, 2020
By Michael Fitzhugh
FDA enforcement of clinical research regulations has often been "light-handed, slow-moving, and secretive," a new look at the agency's enforcement track record concludes. Published today in the journal Science, the analysis said the shortcomings may be harming both patients and trial integrity.
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Regulatory actions for Oct. 1, 2020

Oct. 1, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Abbvie, Aegle, Akari, Baylx, Ionis, Irlab, Kadmon, Pfizer, Provention, Solid, Teneobio, Zosano.
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Regulatory front

Continuing resolution for U.S. budget inked and signed

Oct. 1, 2020
By Mari Serebrov
The latest global regulatory news, changes and updates affecting biopharma, including: FDA finalizes guidance for opioid use disorder drug R&D; FDA releases draft guidance for PK models, cancer drugs.
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The Virtual Medtech Conference

Maisel: FDA developing plans for EUA devices for post-pandemic review

Sep. 30, 2020
By Mark McCarty
The COVID-19 pandemic has not run its course, but the U.S. FDA is already working on a plan for handling devices in the period after the public health emergency ends. Bill Maisel, chief medical officer at the FDA’s Center for Device and Radiological Health (CDRH), said the agency is thinking through what would have to appear in a guidance for a transition that may span a number of months, providing industry with some much-needed breathing room.
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Surgeon wearing headset looks at AR model

FDA clears first holographic cardiac ablation guidance system

Sep. 30, 2020
By Meg Bryant
Sentiar Inc. received U.S. FDA clearance for its holographic guidance system, known as Commandep, for use in cardiac ablation procedures. The system allows electrophysiologists (EPs) to visualize 3D electroanatomic models in real-time, using augmented reality (AR), to seamlessly navigate invasive procedures. “The Commandep is intended for use as a medical imaging system that allows the review, analysis, communication and media interchange of multidimensional digital images,” Berk Tas, Sentiar’s CEO, told BioWorld.
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Regulatory front for Sept. 30, 2020

Sep. 30, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: Cardioquip.
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Regulatory actions for Sept. 30, 2020

Sep. 30, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Becton Dickinson, Genetron, Ka Imaging, Perkinelmer, Sentiar, Vexos.
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Rx pricing hearing highlights U.S. policy divide, gaps in understanding

Sep. 30, 2020
By Mari Serebrov
Rather than the in-your-face, blame-and-shame show that was expected, the Sept. 30 drug pricing hearing before the U.S. House Oversight Committee was more a reminder of the policy differences between Democrats and Republicans on how best to make prescription drugs more affordable.
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Regulatory actions for Sept. 30, 2020

Sep. 30, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: CTI, Diurnal, I-Mab, Iterum, Janssen, Johnson & Johnson, Lantheus, Regenxbio.
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FDA approves Xeljanz for active polyarticular course juvenile idiopathic arthritis

Sep. 30, 2020
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