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Difficulties in incorporating new technologies into existing healthcare systems without disrupting operations or workflows.
Unpredictable availability of medical supplies and devices due to a lack of real-time visibility in supply chain management.
Long wait times and poor scheduling lead to reduced patient satisfaction and overall experience in healthcare settings.
Lengthy approval processes for new medical devices due to complex documentation and compliance requirements.
Maintaining consistent quality across manufacturing processes while adhering to stringent regulatory standards.
Ongoing requirements for monitoring device performance after-market release, necessitating robust data collection.
Difficulties in handling large volumes of data generated during trials, impacting accuracy and compliance with data protection laws.
Resistance to adopting new technologies within clinical trial frameworks, hindering operational efficiency and innovation.
Challenges in ensuring participant safety throughout the trial process due to inadequate real-time monitoring systems.
Maintaining accurate UDI details requires ongoing updates as products change or new devices are introduced into the market.
Difficulties in ensuring effective coordination across the supply chain for accurate tracking and identification of devices.
Complications arising from integrating UDI into existing legacy systems that may not support modern identification standards.
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