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BioWorld - Saturday, February 21, 2026
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Regulatory front for Sept. 11, 2020

Sep. 11, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies.
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Other news to note for Sept. 11, 2020

Sep. 11, 2020
Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Alliancerx Walgreens Prime, Bruker, Canopy Biosciences, Clearside Medical, Collective Medical, Fio, Genetic Technologies, Intelelabs, Intersect ENT, Natera, NaviFUS, Nebraska Health Information Initiative, Noridian Healthcare Solutions, Relay Medical, Todos Medical, Veracyte, Xifin.
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Health professional holding stethoscope with health icons

Drop in clinical news likely related to earlier COVID-19 delays

Sep. 11, 2020
By Karen Carey
The volume of clinical data reported throughout the summer has continued to fall, with only 267 items collected in August, a drop of 10% from July and the lowest amount within the last five months.
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Regulatory actions for Sept. 11, 2020

Sep. 11, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Appili, Immupharma, Junshi, Seres, Sol-Gel.
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Other news to note for Sept. 11, 2020

Sep. 11, 2020
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Amyris, Biocomo, Editas, Harbour, Hualan, Johnson & Johnson, Lavvan, Medicinova, VBL.
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In the clinic for Sept. 11, 2020

Sep. 11, 2020
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Anavex, Aura, Atara, Bicycle, Biogen, Cancer Prevention, Celltrion, Clene, Galapagos, Genentech, GW, Immunic, Lilly, Lyra, Neurocrine, Novartis, Partner, Prothena, Reveragen, Santhera, Voyager.
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Microscope and coronavirus illustration

Shuren, Stenzel reiterate plea for LDT legislation in NEJM editorial

Sep. 10, 2020
By Mark McCarty
The rescission order directing the U.S. FDA to abandon regulation of lab-developed tests is scarcely three weeks in the past, but two senior managers at the FDA are pushing back in an editorial appearing in the New England Journal of Medicine. The FDA’s Jeff Shuren and Tim Stenzel wrote that there is “a need for a common legislative framework” to ensure clinical tests are accurate and reliable, which implicitly concedes that the statute does not authorize the agency to regulate lab-developed tests.
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BioWorld MedTech’s Diagnostics Extra for Sept. 10, 2020

Sep. 10, 2020
By Meg Bryant and Anette Breindl
Keeping you up to date on recent developments in diagnostics, including: Deep learning aid for diagnosing TB in HIV patients; Self-collected swabs vs. health care worker collected for COVID-19 testing; SCAD vs. plaques in heart attacks; Diagnosing neuroblastoma in children.
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Regulatory actions for Sept. 10, 2020

Sep. 10, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Boston Scientific, Exsomed, Glaxosmithkline, Innoviva, Izi Medical, Verily.
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Other news to note for Sept. 10, 2020

Sep. 10, 2020
Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: 1Health.io, Acto Technologies, Aesthetic Solutions, Alesi Surgical, Ambra Health, Cerner, Change Healthcare, Covi-ID, Diopsys, Francophone Federation of Digestive Oncology, Haliodx, Inspiremd, Jilin Changchun Haoyue Halal Meat Live Media Group, Lumithera, Medtronic, Olympus, Pathcheck Foundation, Qt Ultrasound, Safesite, Securehealth, Scrimmage, Skylinedx, Soliton, Tcl Healthcare Equipment, Varian, Venus Medical, Workcare.
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