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HHS Says Memo Won’t Take Power From the FDA

  • Post author:Sam
  • Post published:September 20, 2020
  • Post category:Devices & Diagnostics Letter

HHS on Sunday refuted reports that a new departmental memo will take decision-making power away from the FDA regarding the approval of COVID-19 vaccines or therapeutics. Source: Devices & Diagnostics…

Continue ReadingHHS Says Memo Won’t Take Power From the FDA

State Treasurers Accuse Gilead of Seeking ‘Unreasonable Profits’ From Remdesivir

  • Post author:Sam
  • Post published:September 20, 2020
  • Post category:Devices & Diagnostics Letter

In a letter to Gilead Sciences, almost a dozen state treasurers accused the company of seeking “unreasonable profits” from its antiviral COVID-19 treatment remdesivir, demanding that it lower the price.…

Continue ReadingState Treasurers Accuse Gilead of Seeking ‘Unreasonable Profits’ From Remdesivir

Russian COVID-19 Therapeutic Coronavir to Hit Pharmacy Shelves in Coming Days

  • Post author:Sam
  • Post published:September 20, 2020
  • Post category:Devices & Diagnostics Letter

Coronavir, a treatment developed by Russian company R-Pharm for mild-to-moderate COVID-19 infections, is slated to be offered in pharmacies in that country as early as this week. Source: Devices &…

Continue ReadingRussian COVID-19 Therapeutic Coronavir to Hit Pharmacy Shelves in Coming Days

EU Signs COVID-19 Vaccine Supply Deal With Sanofi/GSK

  • Post author:Sam
  • Post published:September 20, 2020
  • Post category:Devices & Diagnostics Letter

In the European Union’s (EU) latest move to secure supplies of a COVID-19 vaccine, the European Commission (EC) has signed a contract with Sanofi and GlaxoSmithKline (GSK) for 300 million…

Continue ReadingEU Signs COVID-19 Vaccine Supply Deal With Sanofi/GSK

EMA Expert Group Recommends Dexamethasone for COVID-19

  • Post author:Sam
  • Post published:September 20, 2020
  • Post category:Devices & Diagnostics Letter

The corticosteroid dexamethasone has earned the blessing of the EMA’s Committee for Medicinal Products for Human Use (CHMP) for treating COVID-19 patients who require oxygen therapy. Source: Devices & Diagnostics…

Continue ReadingEMA Expert Group Recommends Dexamethasone for COVID-19

Roche’s Actemra Cuts Ventilator Need in COVID-19 Patients

  • Post author:Sam
  • Post published:September 20, 2020
  • Post category:Devices & Diagnostics Letter

Roche’s late-stage COVID-19 trial of Actemra (tocilizumab) showed the rheumatoid arthritis drug reduced the number of coronavirus patients who progressed to mechanical ventilation, suggesting it might be of benefit as…

Continue ReadingRoche’s Actemra Cuts Ventilator Need in COVID-19 Patients

Lawmakers Lash Out at White House Over Hahn Testimony on COVID-19

  • Post author:Sam
  • Post published:September 20, 2020
  • Post category:Devices & Diagnostics Letter

Leaders of the House Energy and Commerce committee on Friday lashed out at the Trump administration for allegedly blocking Commissioner Stephen Hahn from testifying about the agency’s COVID-19 response. Source:…

Continue ReadingLawmakers Lash Out at White House Over Hahn Testimony on COVID-19

DiaSorin’s COVID-19 Test Gets European OK for Saliva Samples

  • Post author:Sam
  • Post published:September 20, 2020
  • Post category:Devices & Diagnostics Letter

The direct molecular test received an initial FDA Emergency Use Authorization in March. Source: Devices & Diagnostics Letter

Continue ReadingDiaSorin’s COVID-19 Test Gets European OK for Saliva Samples

Abbott’s Over-the-Counter Sport Glucose Sensor Gains CE Mark

  • Post author:Sam
  • Post published:September 20, 2020
  • Post category:Devices & Diagnostics Letter

Athletes place the small round biosensor on the back of an upper arm. Source: Devices & Diagnostics Letter

Continue ReadingAbbott’s Over-the-Counter Sport Glucose Sensor Gains CE Mark

Trump Criticizes FDA Delay of Convalescent Plasma EUA

  • Post author:Sam
  • Post published:August 20, 2020
  • Post category:Devices & Diagnostics Letter

President Trump is lashing out at the FDA’s decision to hold off issuing an Emergency Use Authorization (EUA) for using convalescent plasma to treat COVID-19 patients. Source: Devices & Diagnostics…

Continue ReadingTrump Criticizes FDA Delay of Convalescent Plasma EUA
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