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BioWorld - Sunday, February 1, 2026
Home » Topics » Regulatory

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Cybersecurity data lock

Culture of scientific exchange seen as a risk factor for life science cybersecurity

July 22, 2020
By Mark McCarty
The U.S. government has charged two citizens of China with cybercrime in connection with purported hacking of research into vaccines for the SARS-CoV-2 virus, but more than one speaker on a July 22 webinar said scientists involved in basic life science research at universities fail to appreciate the need for cybersecurity, a problem they may take with them to the private sector.
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Green traffic light

Micro-X gets FDA green light for Rover mobile X-ray for military medical use

July 22, 2020
By Tamra Sami
PERTH, Australia – The U.S. FDA gave the thumbs up to Australia’s Micro-X Ltd. for its Rover mobile X-ray system. The 510(k) application was cleared in just five weeks. The concept for the Rover was originally developed under a contract with the Australian Department of Defense to prove that Micro-X’s technology could fulfill an unmet need for a full performance, digital medical X-ray imager that was light enough to be used in deployed medical facilities.
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Regulatory front for July 22, 2020

July 22, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: Cordant, MITA.
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Regulatory actions for July 22, 2020

July 22, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Becton Dickinson, Canon Medical, Cerapedics, Integra, X-Nav Technologies.
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Wake-up call: FDA approves excessive daytime sleepiness treatment from Jazz

July 22, 2020
By Lee Landenberger
The FDA has approved Xywav (calcium, magnesium, potassium and sodium oxybates; JZP-258), an oxybate product for treating both cataplexy and excessive daytime sleepiness in narcolepsy patients ages 7 and older, from Jazz Pharmaceuticals plc.
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Technical difficulties illustration

Virtual meetings bring new challenges to adcoms

July 22, 2020
By Mari Serebrov
Interludes of classical music. Little kids talking in the background. Unmuted mics as panelists multitask. Gurgles of “underwater” sound. Periods of silence as speakers forget to unmute. And then the technical problems – lots of them. Such are the challenges of addressing a virtual FDA advisory committee in the time of COVID-19.  
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Regulatory actions for July 22, 2020

July 22, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Aurinia, AGTC, Jazz, MC2, Redhill.
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Regulatory front for July 22, 2020

July 22, 2020
The latest global regulatory news, changes and updates affecting biopharma, including: Intercept, Sangamo, Stason, Signa.
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FDA approves Qutenza for neuropathic pain associated with DPN of the feet

July 22, 2020
Flag of India

Biocon’s repurposed psoriasis drug gets Indian approval for COVID-19

July 21, 2020
By T.V. Padma
NEW DELHI – Bangalore-based Biocon Ltd. has received the Indian drug regulator's approval for restricted emergency use of its psoriasis biologic, itolizumab, to treat patients with severe cases of COVID-19 in need of ventilator support.
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