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Why FDA Accepts ‘True Copies’ of Records During Inspections

  • Post author:PacConAdmin
  • Post published:August 14, 2024
  • Post category:Uncategorized
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This excerpt is from the management report titled “Managing Data and Documentation for FDA Inspections and Remote Assessments,” based on a webinar from FDAnews, a WCG Clinical company. The presenter…

Continue ReadingWhy FDA Accepts ‘True Copies’ of Records During Inspections

Warning Letter Walkthrough: Making Monitoring, Site Activation Top Priorities

  • Post author:PacConAdmin
  • Post published:August 14, 2024
  • Post category:Uncategorized
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A recent FDA Warning Letter illustrates to sponsors the importance of properly managing monitoring responsibilities and having a thorough site activation process. In this article, we’ll examine the letter received…

Continue ReadingWarning Letter Walkthrough: Making Monitoring, Site Activation Top Priorities

Abiomed Recalls Certain Impella Devices Due to Inspection Failures

  • Post author:PacConAdmin
  • Post published:August 14, 2024
  • Post category:Uncategorized
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Abiomed has recalled certain Impella CP with SmartAssist heart pumps after nine devices in a single lot failed a company inspection — but were inadvertently released to customers — the…

Continue ReadingAbiomed Recalls Certain Impella Devices Due to Inspection Failures

After Clearing CRL, ARS Wins FDA Approval of First Nasal Spray for Anaphylaxis

  • Post author:PacConAdmin
  • Post published:August 14, 2024
  • Post category:Uncategorized
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After a bumpy road to approval, the FDA has approved ARS Pharmaceuticals’ neffy (epinephrine nasal spray) for the emergency treatment of Type I allergic reactions, including those that are life-threatening…

Continue ReadingAfter Clearing CRL, ARS Wins FDA Approval of First Nasal Spray for Anaphylaxis

Quick Notes: Medical Device Clearances — Aug. 13, 2024

  • Post author:PacConAdmin
  • Post published:August 13, 2024
  • Post category:Uncategorized
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This edition of Quick Notes features clearances for a mini robotic system, peripheral arterial disease and peripheral vascular disease testing devices, testing assays for the evaluation of monoclonal gammopathy and…

Continue ReadingQuick Notes: Medical Device Clearances — Aug. 13, 2024

FDA Publishes Pair of Cancer Drug Development Guidances

  • Post author:PacConAdmin
  • Post published:August 13, 2024
  • Post category:Uncategorized
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The FDA has issued two new guidances on the development of oncology drugs and biologics, posting a final guidance on optimizing cancer drug doses and a draft guidance on developing…

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Semaglutide Use Increases More than 400 Percent in Three Years, Study Says

  • Post author:PacConAdmin
  • Post published:August 13, 2024
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A study of trends in prescriptions dispensed at retail pharmacies for semaglutide showed a 442 percent increase in fills between January 2021 and December 2023 — increasing from 659,000 to…

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CMS’ Emerging Technologies Pathway to Cover up to 5 New Devices a Year

  • Post author:PacConAdmin
  • Post published:August 13, 2024
  • Post category:Uncategorized
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CMS has issued a final procedural notice outlining a Medicare coverage pathway — Transitional Coverage for Emerging Technologies (TCET) — for certain FDA Breakthrough Devices to be covered under Medicare.…

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Legislative Update — Week of Aug. 12, 2024

  • Post author:PacConAdmin
  • Post published:August 12, 2024
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During the second session of the 118th Congress, FDAnews will track important pending legislation, that has been acted on by Dec. 31, 2023 to keep you updated on laws and…

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Lilly Touts Positive Results from Tirzepatide Clinical Trial

  • Post author:PacConAdmin
  • Post published:August 12, 2024
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Eli Lilly announced positive results from a phase 3 clinical trial evaluating the safety and efficacy of tirzepatide injection in adults with heart failure with preserved ejection fraction and obesity.…

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