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BioWorld - Thursday, June 11, 2026
Home » Topics » Regulatory

Regulatory
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Regulatory actions for April 1, 2022

April 1, 2022
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: CTL Amedica, Radiaction.
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Regulatory actions for April 1, 2022

April 1, 2022
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Akston, Amylyx, Autolus, Cytodyn, Design, Everest Medicines, Gilead Sciences, Glaxosmithkline, JW, Mission, Nordic, Novartis, Novavax, Outlook, Sorrento, Vir, Xortx.
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Man sleeping with CPAP machine

USPSTF may hit snooze button on sleep apnea screening for asymptomatic patients

March 31, 2022
By Mark McCarty
The U.S. Preventive Services Task Force (USPSTF) has decided to consider the merits of screening for obstructive sleep apnea (OSA), a condition thought to contribute significantly to the onset of heart disease. Even though five years have passed since the task force considered the merits of screening for asymptomatic patients, USPSTF indicated that there is still insufficient evidence to support the proposition, citing an evidence gap that if filled could prove tremendously useful to makers of devices that diagnose and treat the condition.
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Securities fraud class actions still a source of cost for life science companies

March 31, 2022
By Mark McCarty
Publicly traded companies in the life sciences face a number of sources of litigation, including lawsuits over alleged securities fraud, and a new report by Dechert LLP highlights a diminishing number of such lawsuits across the U.S. economy. However, the proportion of such lawsuits directed at drug and device makers has not diminished, making clear that companies in the life sciences must tread carefully when disclosing information such as the status of products in development for fear that a perceived misrepresentation could spark expensive and time-consuming litigation.
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EU issuing wartime advice on clinical trials

March 31, 2022
By Mari Serebrov
With the Russian invasion of Ukraine continuing to disrupt thousands of clinical trials throughout the region, the European Commission, the EMA and the Heads of Medicines Agencies are developing advice to help sponsors mitigate the issues.
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FDA icons

ViVA la (non-)difference: Akebia eager for FDA sit-down re vadadustat CRL

March 31, 2022
By Randy Osborne
The company conference call related to Akebia Therapeutics Inc.’s complete response letter (CRL) for vadadustat, an HIF prolyl-hydroxylase inhibitor for anemia caused by chronic kidney disease, brought on the ongoing and perhaps inevitable comparisons with a similar product from Fibrogen Inc., rejected by the agency last August.
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New shortage threatens Rx supply chain

March 31, 2022
By Mari Serebrov
Throughout the COVID-19 pandemic, biopharma companies across the world have had to deal with shortages resulting from supply chain issues.
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Architectural pillars

US SEC proposal may retract SPAC space

March 31, 2022
By Mari Serebrov
The U.S. SEC is proposing rules that could close off the advantages of going public via a special purpose acquisition company, or SPAC.
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Regulatory actions for March 31, 2022

March 31, 2022
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Edwards.
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Regulatory actions for March 31, 2022

March 31, 2022
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Abionyx, Antengene, ASC, Biogen, Guerbet, Hipra, Nurix, Realta, Receptor, Taiho, Viiv.
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