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BioWorld - Sunday, June 14, 2026
Home » Topics » Regulatory

Regulatory
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Clinical data up 30% over last year; a fifth focused on COVID-19

March 15, 2021
By Karen Carey
After a year of intense biopharma research, an increasing arsenal of answers is bolstering the fight against COVID-19.
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Regulatory actions for March 15, 2021

March 15, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Bioxcel, Calliditas, Histogen, Melinta, Oryzon, Pharmaessentia, Tetra.
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Regulatory front

EMA weighing blood clot data

March 15, 2021
By Mari Serebrov
The latest global regulatory news, changes and updates affecting biopharma, including: FDA launches EUA safety dashboard; Fed Circuit claims mandamus jurisdiction in IPR institution; Comment period reopened on Orange Book patents.
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U.S. FDA headquarters

Compliance sticker shock may await EUA holders new to device space

March 12, 2021
By Mark McCarty
Most of the med-tech companies doing business during the COVID-19 pandemic are experienced and already have their FDA compliance systems in place. However, Dennis Gucciardo, a partner at the D.C. office of Morgan, Lewis & Bockius LLP, told BioWorld that while the FDA will give industry sufficient time to transition their emergency use authorizations (EUAs) to conventional premarket filings, the cost of setting up a quality management system may be greater than some current EUA holders are willing to bear.
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Regulatory front for March 12, 2021

March 12, 2021
By Mark McCarty
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: FDA announces recall of infusion sets; Recall announced for Roche testing systems; NIH announces technique for improved photoreceptor imaging.
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Regulatory actions for March 12, 2021

March 12, 2021
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Baxter.
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Green approved stamp

Remegen wins China approval for lupus drug telitacicept

March 12, 2021
By Elise Mak
Remegen Co. Ltd.’s RC-18 (telitacicept) was granted conditional approval for systemic lupus erythematosus (SLE), marking the first NDA approval for the company that launched the world’s biggest biotech IPO last year.
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NME approvals and COVID-19 regulatory data rise in February

March 12, 2021
By Karen Carey
FDA approvals in February nearly doubled those of the prior month, although biopharma regulatory data, aside from efforts targeting COVID-19, continue to decline.
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Regulatory actions for March 12, 2021

March 12, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Eisai, J&J, RDIF, Sanofi, Takeda.
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Drug vial and syringe

EMA: Blood clot investigation continues, vaccine safe so far

March 12, 2021
By Mari Serebrov
What started with Austrian regulators suspending use of one batch of Astrazeneca plc’s COVID-19 vaccine has expanded into precautionary holds in Denmark and other EU countries as PRAC, the EMA’s safety committee, investigates whether blood clots, which have resulted in at least two deaths in Europe, are connected to the vaccine.
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