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BioWorld - Thursday, July 16, 2026
Home » Topics » Regulatory

Regulatory
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U.S. flag on columned building

2020 Special 301 report calls out the usual U.S. trade partners for IP offenses

April 29, 2020
By Mari Serebrov
Saudi Arabia, which last year made its first appearance on the U.S. Trade Representative’s (USTR) Priority Watch List, is back on the list this year and is being singled out for an out-of-cycle review due to what the USTR calls its “unfair commercial use” and “unauthorized disclosure” of proprietary data submitted for drug approvals.
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Wall Street hails Chimerix viral load; COVID-19, smallpox bids forge onward

April 29, 2020
By Randy Osborne
A pair of good-news items from Chimerix Inc. pushed the Durham, N.C.-based company’s stock (NASDAQ:CMRX) to $2.15, closing up 64 cents, or 42%, higher as backers reacted to near-term NDA plans for smallpox countermeasure brincidofovir (BCV) and the start of a phase II/III trial with dociparstat sodium (DSTAT) in COVID-19 patients with acute lung injury (ALI).
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Regulatory front for April 29, 2020

April 29, 2020
The latest global regulatory news, changes and updates affecting biopharma.
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Regulatory actions for April 29, 2020

April 29, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Algernon, Amylyx, ANI, Azurrx, Beyondspring, Capricor, Chimerix, Erytech, Merck, Neuraptive, Novartis, Ortho Dermatologics, Remegen.
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Lungpacer-DPTS-device.png

Lungpacer wins EUA for device to wean patients off ventilators

April 28, 2020
By Meg Bryant
Reports of unusually high death rates for COVID-19 patients on ventilators have raised alarms, and some doctors are looking to reduce reliance on the breathing machines when possible. To advance that goal, Lungpacer Medical Inc., of Vancouver, British Columbia, has obtained an emergency use authorization (EUA) from the U.S. FDA for its Lungpacer diaphragmatic pacing therapy system (DPTS) for immediate use in ventilator patients at high risk of weaning failure, including patients with the novel coronavirus.
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Regulatory front for April 28, 2020

April 28, 2020
The latest global regulatory news, changes and updates affecting biopharma, including: Biomedical Advanced Research and Development Authority, COVID-19 EMA Pandemic Task Force, Cybersecurity and Infrastructure Security Agency, EMA, European Commission, FDA, Heads of Medicines Agencies, National Institute for Health and Care Excellence, NIH, Therapeutic Goods Administration, U.S. Cyber Command, U.S. House and Senate, Wuhan Institute of Virology.
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Regulatory front for April 28, 2020

April 28, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: Health Quality Ontario, Imagination Engines.
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Regulatory action for April 28, 2020

April 28, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Chronolife, Edwards Lifesciences, Exthera, Icecure, Life Spine, Lungpacer Medical, Medipines.
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Regulatory actions for April 28, 2020

April 28, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Adaptimmune, Bioeclipse, Moderna, Moleculin, Pharmamar, Retrotope, Roche, Sanofi, Shionogi, Zambon.
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Regulatory front for April 28, 2020

April 28, 2020
The latest global regulatory news, changes and updates affecting biopharma, including: Chugai, Fresenius, Genentech, Pfizer, Quva, Roche, Vertex.
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