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BioWorld - Wednesday, July 1, 2026
Breaking News: Science fiction realized: BCI tech is hereBreaking News: Science fiction realized: BCI tech is here
Home » Topics » BioWorld, Regulatory

BioWorld, Regulatory
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Regulatory actions for Feb. 19, 2021

Feb. 19, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Dr. Reddy’s, Dynavax, Immunicum, Immunocore, Incyte, Janssen-Cilag, Junshi, RDIF, Travere.
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Regulatory front

CRS says user fee shares of total review costs on the rise

Feb. 19, 2021
The latest global regulatory news, changes and updates affecting biopharma.
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Oral medication

Athenex specs checked as Oraxol awaits PDUFA date

Feb. 18, 2021
By Randy Osborne
Athenex Inc.’s launch of Klisyri (tirbanibulin) likely whetted investor appetite for another prospect coming down the pike: Oraxol, an oral form of paclitaxel for which the Buffalo, N.Y.-based firm has been assigned a PDUFA date of Feb. 28.
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Regulatory actions for Feb. 18, 2021

Feb. 18, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Astellas, Avacta, CNS, Seagen, WPD.
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U.K. flag on stethoscope

U.K.’s MHRA requires trial sponsors to assess vaccine impact

Feb. 17, 2021
By Mari Serebrov
In a Feb. 17 update to its guidance on managing clinical trials during the COVID-19 pandemic, the U.K.’s Medicines and Healthcare Products Regulatory Agency (MHRA) said all sponsors of ongoing clinical trials for indications other than treatment or prevention of COVID-19 are required to evaluate the impact a COVID-19 vaccine may have on the trial.
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2021 BIO CEO & Investor Conference

Machine learning IDs indication, modality, biomarkers as top predictors of clinical success

Feb. 17, 2021
By Jennifer Boggs
Investing in biopharma has never been for the faint of heart. So headline figures unveiled from a clinical development success report during the BIO CEO & Investor Conference Feb. 17, putting the average likelihood of a drug entering phase I development ultimately achieving approval at 7.9% and the average drug development timeline at 10.5 years, appear largely unsurprising. But the addition of machine learning capabilities to the mix helped identify those factors that have the greatest impact on predictive outcome.
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Australia establishes COVID-19 vaccine safety monitoring plan ahead of rollout

Feb. 17, 2021
By Tamra Sami
PERTH, Australia – With the first COVID-19 vaccine ready to be launched in Australia, the Therapeutic Goods Administration has released guidance on its pharmacovigilance plan to track real-world safety data and adverse events following immunization.
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Regulatory actions for Feb. 17, 2021

Feb. 17, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Altimmune, Amgen, Beigene, Coherus, JCR, Johnson & Johnson, Novartis, RDIF, Ultragenyx, Verrica.
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Australia and coronavirus syringe

Australia’s TGA grants provisional approval to Astrazeneca’s COVID-19 vaccine

Feb. 16, 2021
By Tamra Sami
PERTH, Australia – Australia’s Therapeutic Goods Administration (TGA) has granted provisional approval to Astrazeneca Pty Ltd. for its COVID-19 vaccine, a recombinant adenovirus vaccine, making it the second COVID-19 vaccine to receive regulatory approval in Australia, following the Jan. 26 provisional approval for Pfizer Australia Pty Ltd.’s COVID-19 vaccine, branded Comirnaty.
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G1 Therapeutics gains first FDA nod with myelopreservation therapy Cosela

Feb. 16, 2021
By Jennifer Boggs
As expected, G1 Therapeutics Inc.’s Cosela (trilaciclib) won FDA approval for use in extensive-stage small-cell lung cancer patients undergoing chemotherapy, becoming the first proactively administered myelopreservation therapy to hit the market.
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