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BioWorld - Saturday, May 16, 2026
Home » Topics » Infection » Coronavirus

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Regulatory actions for Dec. 11, 2020

Dec. 11, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Arix, Biogen, Bristol Myers Squibb, Daiichi Sankyo, Dynavax Technologies, Excellthera, Gilead Sciences, Janssen, Lexicon, Merck, Passage, Sanofi, Seagen, Soleno, V2act, Viiv Healthcare, Xeris.
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Other news to note for Dec. 11, 2020

Dec. 11, 2020
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Active, Astrazeneca, Bristol Myers, Cipla, Fera, Immunitybio, Immunoprecise, Innate, Medivir, Neotx, Pear, Polyphor, Quralis, Tetralogic.
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In the clinic for Dec. 11, 2020

Dec. 11, 2020
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Akari, Geron, Greenwich Lifesciences, Mitsubishi Tanabe, Prevail, Puma, Puretech Health, Scyneis, Sellas Life Sciences, Tychan.
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Vaccine administration

Vaccine EUA not a total slam dunk with adcom

Dec. 10, 2020
By Mari Serebrov
The FDA’s vaccine advisory committee voted 17-4 with one abstention Dec. 10 to recommend an emergency use authorization (EUA) for the Pfizer Inc./Biontech SE mRNA vaccine BNT-162b2 to prevent COVID-19 in individuals 16 and older.
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Elecsys Anti-SARS-COV-2 packaging

Roche teams up with Moderna for vaccine trials

Dec. 10, 2020
By Liz Hollis
Roche Holding AG has revealed a partnership with Moderna Inc. involving the use of the Elecsys Anti-SARS-CoV-2 S antibody test in the latter’s mRNA-1273 vaccine research trials. The news comes shortly after Roche received emergency use authorization from the U.S. FDA for the antibody test. 
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Pixel by LabCorp

Labcorp snags EUA for first direct-to-consumer COVID-19 test

Dec. 10, 2020
By Meg Bryant
The U.S. FDA has made it easier for people who want to get tested for COVID-19, granting emergency use authorization (EUA) for direct-to-consumer sales of Laboratory Corp. of America Holdings’ (Labcorp) Pixel COVID-19 test home collection kit. With this latest EUA, any individual 18 years and older can purchase the Pixel test system without a prescription.
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BioWorld MedTech’s Diagnostics Extra for Dec. 10, 2020

Dec. 10, 2020
By Meg Bryant and Anette Breindl
Keeping you up to date on recent developments in diagnostics, including: Predicting breast cancer recurrence, Comparing SARS-CoV-2 PCR tests, Paying attention to the little guy in proteomics, Increasing biomarker reproducibility
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Regulatory front

House passes stopgap spending bill

Dec. 10, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: Senate passes counterfeit device destruction bill; MHRA posts device compliance dates for Brexit.
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Regulatory actions for Dec. 10, 2020

Dec. 10, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Advanced Bionics, Advanced Medtech, Laboratory Corporation of America, Oxford Immunotec Global, Recor Medical, Virocule.
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Other news to note for Dec. 10, 2020

Dec. 10, 2020
Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Anade, Applied Biosystems, Aural Analytics, Corvion, Cytosorbents, Diagnosticos da America, Establishment Labs Holdings, Everheart Systems, First Nation Group, Fresenius, Globus Medical, Haliodx, Irras, Lucence, Microport Cardio Rhythm Management, Nightware, Novocure, Rewalk Robotics, Sectra, Stata Oncology, Thermo Fisher Scientific, Tridiuum, Twist Bioscience, Viveve Medical, Vivos.
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