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Biden’s Price Controls Will Hinder U.S. Clinical Research, Chamber of Commerce Says

  • Post author:PacConAdmin
  • Post published:December 12, 2023
  • Post category:Uncategorized

Actions and future plans by the Biden administration to impose drug price controls could prove disastrous for U.S. clinical trials and medical innovation overall, the U.S. Chamber of Commerce (CoC)…

Continue ReadingBiden’s Price Controls Will Hinder U.S. Clinical Research, Chamber of Commerce Says

Peptide Guidance Comments Stress Categorization, Immune Responses

  • Post author:PacConAdmin
  • Post published:December 12, 2023
  • Post category:Uncategorized

Comments from AstraZeneca, Pfizer, Johnson & Johnson and Certara on the FDA’s draft guidance on developing peptide drugs focused on ways to categorize peptides and the potential for the drugs…

Continue ReadingPeptide Guidance Comments Stress Categorization, Immune Responses

FTC Issues Complaint Against Sanofi/Maze Acquisition Deal; Sanofi Caves

  • Post author:PacConAdmin
  • Post published:December 12, 2023
  • Post category:Uncategorized

The FTC announced on Monday its intention to block Sanofi’s proposed acquisition of an exclusive license to Maze Therapeutics’ therapy in development for treatment of Pompe disease and hours later…

Continue ReadingFTC Issues Complaint Against Sanofi/Maze Acquisition Deal; Sanofi Caves

AdvaMed Announces New Medical Imaging Technology Division

  • Post author:PacConAdmin
  • Post published:December 12, 2023
  • Post category:Uncategorized

AdvaMed announced the establishment of a new medical imaging technology division that will advocate on behalf of large and small devicemakers, and is establishing itself as the new home for…

Continue ReadingAdvaMed Announces New Medical Imaging Technology Division

Getinge Recall of Cardiohelp Emergency Drive Deemed Class I by FDA

  • Post author:PacConAdmin
  • Post published:December 11, 2023
  • Post category:Uncategorized

Getinge’s recall of its Cardiohelp for problems with its emergency drive has been identified by the FDA as a Class I recall — the most serious type of recall as…

Continue ReadingGetinge Recall of Cardiohelp Emergency Drive Deemed Class I by FDA

Price Hikes for 8 of 10 High-Cost Drugs Not Supported by New Evidence, Says ICER

  • Post author:PacConAdmin
  • Post published:December 11, 2023
  • Post category:Uncategorized

Eight of 10 high-cost drugs — with increases that totaled $1.27 billion — had substantial price increases in 2022 that were not supported by new clinical evidence, a new report…

Continue ReadingPrice Hikes for 8 of 10 High-Cost Drugs Not Supported by New Evidence, Says ICER

Teva Petitions Federal Judge in Colorado to Reject Motion to Dismiss Epi-Pen Lawsuit

  • Post author:PacConAdmin
  • Post published:December 11, 2023
  • Post category:Uncategorized

Teva Pharmaceuticals has asked a Colorado federal judge to keep alive its lawsuit challenging the state’s epinephrine auto-injector (epi-pen) affordability program as unconstitutional, arguing that suing in state court for…

Continue ReadingTeva Petitions Federal Judge in Colorado to Reject Motion to Dismiss Epi-Pen Lawsuit

HHS Releases Fall 2023 Unified Agenda

  • Post author:PacConAdmin
  • Post published:December 11, 2023
  • Post category:Uncategorized

HHS’s fall unified agenda of proposed rules for the FDA includes a new rule that revokes two old rules that have either been superseded or do not reflect current agency…

Continue ReadingHHS Releases Fall 2023 Unified Agenda

Legislative Update — Week of Dec. 11, 2023

  • Post author:PacConAdmin
  • Post published:December 11, 2023
  • Post category:Uncategorized

As the first session of the 118th Congress continues, FDAnews will track important pending legislation, that has been acted on since July 1, to keep you updated on laws and…

Continue ReadingLegislative Update — Week of Dec. 11, 2023

Devicemaker IVDR Application Foot-Dragging Shown in Team NB Survey

  • Post author:PacConAdmin
  • Post published:December 8, 2023
  • Post category:Uncategorized

A survey conducted among attendees of Team NB’s second in vitro device regulation (IVDR) training seminar reflected the worrisome trend of foot-dragging among manufacturers in making an application to a…

Continue ReadingDevicemaker IVDR Application Foot-Dragging Shown in Team NB Survey
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