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BioWorld - Wednesday, July 8, 2026
Home » Topics » Regulatory

Regulatory
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Sarepta wins accelerated FDA approval for third DMD therapy, casimersen

Feb. 25, 2021
By Michael Fitzhugh
As expected, the FDA granted an approval for Amondys 45 (casimersen), a new Duchenne muscular dystrophy (DMD) therapy developed by Sarepta Therapeutics Inc.
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Lack of clinical trial diversity could have consequences

Feb. 25, 2021
By Mari Serebrov
Drug and device companies dragging their feet on diversifying late-stage clinical trials could conceivably get a wake-up call in court or in FDA approval delays. A final guidance the FDA released in November suggests that the days of ignoring segments of the intended treatment population until safety signals flare in real-world use are coming to an end.
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Regulatory front for Feb. 25, 2021

Feb. 25, 2021
The latest global regulatory news, changes and updates affecting biopharma.
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Regulatory actions for Feb. 25, 2021

Feb. 25, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Abbvie, Aquestive, Bluebird, Cansino, Exelixis, Gannex, J&J, Retrotope, RDIF, Sinopharm, Viiv.
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Map of Latin America, South America

COVID-19 pandemic charges Latin American med-tech sector

Feb. 24, 2021
By Sergio Held
CAJICA, Colombia – Three countries have emerged as the key engines of growth for Latin America’s medical devices sector, accounting for the largest share of exports and investment in the space across the region and experiencing growth over the past decade that may have been supercharged by the COVID-19 pandemic.
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Harvard’s Mina blasts FDA as bottleneck in rapid testing dust-up

Feb. 24, 2021
By Mark McCarty
The U.S FDA’s response to the pandemic has been all-consuming, but epidemiologist Michael Mina of Harvard blasted the agency’s handling of rapid testing. Mina said the agency is in possession of emergency use authorization filings for rapid antigen tests that should be acceptable, but that the FDA is “the only bottleneck” in the rapid antigen testing pipeline.
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Regulatory actions for Feb. 24, 2021

Feb. 24, 2021
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Agilent, Assure Tech, Dascena, G21, Locate Bio.
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Regulatory front for Feb. 24, 2021

Feb. 24, 2021
By Mark McCarty
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: ACLA sees need for clarification of test coverage; MITA seeks transparency at USPSTF; NIH eyes license for cancer therapy; GAO says federal agencies falling short on recommendations; TGA updates guidance for risks in drugs and devices.
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Regulatory front for Feb. 24, 2021

Feb. 24, 2021
The latest global regulatory news, changes and updates affecting biopharma.
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Regulatory actions for Feb. 24, 2021

Feb. 24, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Aim, Antengene, Kura, Pfizer, RDIF, Teleflex.
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