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BioWorld - Friday, March 13, 2026
Home » Topics » Infection » Coronavirus

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BioWorld MedTech’s Orthopedics Extra for Oct. 21, 2020

Oct. 21, 2020
By Holland Johnson
Keeping you up to date on recent developments in orthopedics, including: Magnetic field and hydrogels could be used to grow new cartilage; COVID-19 pandemic has dramatic impact on osteoporosis management, finds new global study; Casting call: Why immobilizing helps in healing; Osteoarthritis biomarker could help 300 million people worldwide.
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Regulatory front

CDC says two-thirds of 2020’s excess deaths due to COVID-19

Oct. 21, 2020
By Mark McCarty
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: Advamed says shipped tests reach 200M mark; Brazil, U.S. expand on 2011 trade handshake; Federal Circuit reaches split decision in review of IPR.
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Regulatory actions for Oct. 21, 2020

Oct. 21, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Acuitive, Appliedvr, Certest, Tyber, Venturemed.
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Other news to note for Oct. 21, 2020

Oct. 21, 2020
Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: 3Shape, Agendia, Align Technology, Guided Therapeutics, Hatch Medical, Infinity Biologix, Philips, Precision Genetics, Rldatix, Royal Philips, Simonmed Imaging, Teladoc Health, Telus Health, Vascutech Medical, Vault Health, Verge Health.
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Other news to note for Oct. 21, 2020

Oct. 21, 2020
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Actinium, Arsenalbio, Astrazeneca, Biomx, Bridgebio, Cannabics, Chromotek, Cidara, Curelab, Curis, Diurnal, Effrx, Epsilogen, Hemoshear, GT, Intelgenx, Kintara, Moleculin, Mybiotics, Neoimmunetech, Neumentum, Noveome, Nuance (Shanghai), PCI, Poseida, Proteintech, Prothena, PTC, Roche, Scynexis, Seqirus, Takeda, Teneobio, Tetra Bio, Tscan, Union, Vir.
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Digital illustration of U.S., coronavirus

FDA iffy on whether labs should file EUA documentation despite agency’s no-review policy

Oct. 20, 2020
By Mark McCarty
The U.S. FDA’s device center has declared it will not review emergency use authorization (EUA) requests for lab-developed tests (LDTs) for the COVID-19 pandemic, but on the agency’s most recent town hall, on Oct. 14, FDA officials were uncertain as to whether labs should file those EUAs, leaving labs in a state of limbo yet again.
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Regulatory actions for Oct. 20, 2020

Oct. 20, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Clinical Enterprise, Ezra, Spectrum Solutions.
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Other news to note for Oct. 20, 2020

Oct. 20, 2020
Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Acumed, Agilent Technologies, Angle, Astrotech, Axonics Modulation Technologies, Bioreference Laboratories, Breathtech, Caire, Carmat, Change Healthcare, Colson Medical, Conextions, Extricare USA, Fineheart, Healthlynked, Helius Medical Technologies, Icad, Incelldx, Intervenn Biosciences, Intraop Medical, Katena Products, Labcorp, Level Ex, Medofficedirect, Micro-Select Instruments, Minnetronix Medical, Osang Healthcare, Osteomed, PADM, Philips, Rewalk Robotics, Sg Blocks, Smith+Nephew, Stanford Medicine, Swedish, The Doc, Vitalhub, Vivosense, Ymir Genomics, Zoll.
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Nonprofit stamp

Pandemic sweeping biopharma nonprofit deals and grants

Oct. 20, 2020
By Karen Carey
COVID-19 continues to dominate biopharma nonprofit collaborations and grants in 2020, with the pandemic accounting for 85% of projected values reported this year, most of which have posted since the start of July.
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Man having temperature check

COVID-19 challenge study to start in the U.K. next year

Oct. 20, 2020
By Nuala Moran
LONDON - The world’s first COVID-19 human challenge trial is due to start in London next year, after the government announced £33.6 million (US$42.5 million) funding for the project. In the initial phase, the aim is to establish the dose of SARS-CoV-2 needed to cause infection and to characterize the immune response to virus. That will lead on to tests of individual COVID-19 vaccines, in which volunteers will be challenged with the effective dose of SARS-CoV-2 one month after inoculation.
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