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BioWorld - Sunday, July 5, 2026
Home » Topics » Infection » Coronavirus

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Regulatory actions for Dec. 30, 2021

Dec. 30, 2021
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Siemens Healthineers.
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Regulatory actions for Dec. 2, 2021

Dec. 30, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Ascentage, Beyondspring, Bionomics, Bioxcel, CTI, Cytodyn, Harmony, Huyabio, Innovent, Merck, Moleculin, Ridgeback, Shenzhen Chipscreen, Secura, Siga, Statera, Surface, Telix, VBI, Zogenix.
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Woman holding smartphone coughing

Resapp’s stand-alone cough counter app cleared in Australia and Europe

Dec. 29, 2021
By Tamra Sami
PERTH, Australia – Australian digital health company Resapp Health Ltd. received clearance from Australia’s Therapeutics Good Administration and CE mark certification in the EU for its stand-alone cough counter application that tracks cough frequency using a smartphone. The class I software as a medical device is the first regulatory approval for such an application, which uses Resapp’s machine learning algorithms to identify cough events from audio recorded using the smartphone’s in-built microphone.
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Other news to note for Dec. 29, 2021

Dec. 29, 2021
Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Aditxt, Co-Defend, Co-Protect, Lucira, Pacbio, Seegene.
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Regulatory actions for Dec. 29, 2021

Dec. 29, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Amylyx, Janssen, Nrx, RDIF, Statera, Tryp.
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Other news to note for Dec. 29, 2021

Dec. 29, 2021
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Astrazeneca, Ionis, Oramed, Oravax, Rational Vaccines, Tan Thanh.
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More work needed on COVID-19 therapies

Dec. 28, 2021
By Mari Serebrov
The U.S. FDA’s emergency use authorization for two oral antivirals to be used to treat individuals at high risk of progressing to severe disease is just one hurdle cleared, as Pfizer Inc.’s Paxlovid and Merck & Co. Inc.-Ridgeback Biotherapeutics Inc.’s molnupiravir still have many more laps to run.
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Russia updates COVID-19 treatment guidelines

Dec. 28, 2021
By Mari Serebrov
The Russian Ministry of Health issued the 14th version of its guidelines on preventing, diagnosing and treating COVID-19 infections. Released Dec. 28, the latest version includes information about the Omicron variant and provides updates on new therapies, including two new oral drugs: Pfizer Inc.’s Paxlovid (nirmatrelvir tablets and ritonavir tablets, co-packaged for oral use) and Merck & Co. Inc.-Ridgeback Biotherapeutics Inc.’s siRNA drug molnupiravir, which will be marketed in Russia as Mir-19.
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Regulatory actions for Dec. 28, 2021

Dec. 28, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Amniotics, Astrazeneca, Cstone, Daiichi, Leo, Novavax, Regor.
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Other news to note for Dec. 28, 2021

Dec. 28, 2021
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Aditxt, Aipharma, Collegium, Dicerna, Immuneoncia, Moderna, Novo Nordisk, Wuxi.
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