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BioWorld - Tuesday, June 23, 2026
Home » Topics » Regulatory

Regulatory
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Regulatory actions for May 7, 2020

May 7, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Bittium, Camber Spine, Grifols, Neumodx, Sherlock Biosciences.
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Regulatory front for May 7, 2020

May 7, 2020
The latest global regulatory news, changes and updates affecting biopharma, including: Roche Holding.
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Regulatory actions for May 7, 2020

May 7, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Ascentage, Bexion, Canbridge, Daiichi, Genelux, Gilead, Immunicum, Nanobiotix, Novartis, Sapience, Twi.
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FDA approves Tabrecta for metastatic NSCLC with METex14

May 7, 2020
Cytosorb product image

Cytosorbents introduces Cytosorb in Mexico

May 6, 2020
By Sergio Held
After a long approval process, Monmouth Junction N.J.-based Cytosorbents Corp. received clearance to bring its Cytosorb blood purification technology to treat cytokine storm and deadly inflammation in critically ill and cardiac surgery patients, to the Mexican market. The COVID-19 pandemic may delay marketing plans to roll-out the product in the Latin American country.
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Antibodies fighting coronavirus

FDA’s Stenzel highlights sensitivity, specificity for COVID-19 antibody testing

May 6, 2020
By Mark McCarty
The U.S. FDA continues to modify its emergency use authorization (EUA) policy for testing for the SARS-CoV-2 virus, although workplace testing is still on the agency’s to-do list. The FDA’s Tim Stenzel noted on a May 6 briefing that serological tests for antibodies must now demonstrate an overall sensitivity of 90% and overall specificity of 95%, a set of standards that might challenge some tests that are available under the EUA policy.
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FDA approves Novartis’ MET inhibitor Tabrecta for NSCLC

May 6, 2020
By Randy Osborne
Novartis AG won accelerated FDA clearance for Tabrecta (capmatinib, formerly INC-280), an oral MET inhibitor, for adult patients with metastatic non-small-cell lung cancer (NSCLC) whose tumors have a mutation that leads to MET exon 14 skipping (METex14) as detected by a companion diagnostic, also given the green light.
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Regulatory front for May 6, 2020

May 6, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies.
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Regulatory actions for May 6, 2020

May 6, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Headsafe, Foundation Medicine, Setpoint Medical.
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Astrazeneca's Farxiga wins FDA approval to reduce heart failure risks

May 6, 2020
By Michael Fitzhugh
With new a FDA approval for a years-old type 2 diabetes drug, Astrazeneca plc's Farxiga (dapagliflozin) has become the first sodium-glucose co-transporter 2 (SGLT2) inhibitor to be approved to reduce the risk of cardiovascular (CV) death and hospitalization for heart failure patients with reduced ejection fraction, a measure of how much blood the left ventricle pumps out with each contraction.
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