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FDA Needs To Undo Incentives For Single-Use Products, Device Reprocessing Expert Says

 
• By Hannah Daniel

Medtech Insight sat down with Dan Vukelich, president and CEO of the Association of Medical Device Reprocessors, to discuss the need for sustainable alternatives to limit waste from medical devices.

• Source: Shutterstock

A majority of Dan Vukelich’s day-to-day is spent educating manufacturers on the regulatory incentives against reprocessing devices.

“Single-use labeling isn't decided by FDA, it's up to the manufacturer,” the president and CEO of the Association of Medical Device Reprocessors explained in an interview with Medtech Insight.

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FDA Scrubs ‘Gender’ From Final Guidance On Sex-Specific Data But Encourages More Women In Clinical Trials

 
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Swiss Medtechs Advised To Work On US Tariff Mitigation Strategies

 
• By Ashley Yeo

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FDLI: Clinical Labs Face Uncertainty After Texas Court’s LDT Ruling

 
• By Elizabeth Orr

A Texas court's decision against US FDA regulation of lab-developed tests (LDTs) has introduced new uncertainties for clinical labs. Industry stakeholders are now worried about potential future regulations while also managing existing compliance requirements. Recent conference discussions underscored the complexities of FDA oversight.