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The role of real-world evidence in the lifecycle of diagnostic, medical device, and digital therapeutic products

Clarify Health

From FDA regulatory approvals to commercialization strategies to value demonstrations, real-world evidence (RWE) plays a pivotal role in the product lifecycle of diagnostics, medical devices, and digital therapeutics (DTx).

Medical 52
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The role of real-world evidence in the lifecycle of diagnostic, medical device, and digital therapeutic products

Clarify Health

From FDA regulatory approvals to commercialization strategies to value demonstrations, real-world evidence (RWE) plays a pivotal role in the product lifecycle of diagnostics, medical devices, and digital therapeutics (DTx). health systems, IDNs, payers, HCPs, patients) and demonstrate that value to them.

Medical 52
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Medtech’s iPhone Moment: Pioneering Patient Experience-Focused Design in Medical Devices

MedCity News

Flexible, portable medical diagnostic devices are the future, augmenting equity and access to quality healthcare. That means designing for patients as well as caregivers, creating devices that are intuitive, easy to use, and easily adaptable to various environments.

Medical 108
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Perspectum Completes $55M Series C to Improve Metabolic Disease Diagnosis

MedCity News

Perspectum — a company that makes medical imaging devices designed to improve the diagnosis of metabolic diseases and cancer — recently announced the second close of its $55 million Series C funding round. Its flagship product is a diagnostic tool that assesses and monitors chronic liver disease.

Medical 108
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Sparrow BioAcoustics Launches Software That Turns a Smartphone into a Stethoscope 

Legacy MEDSearch

Sparrow BioAcoustics recently unveiled its Stethophone TM software, which transforms smartphones into medical-grade stethoscopes. This innovative tool enables users to capture, analyze, and share crucial heart health data with medical professionals from any location.

FDA 52
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Revised ISO guideline highlights toxicological evaluation of extractables and leachables

European Pharmaceutical Review

In the published in 2023, the process and requirements for toxicological risk assessment of medical device constituents is outlined. The paper discussed the detection of volatile extractables released during the clinical use of medical devices.

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The Future of Medical Device Specialists: Adapting to Industry Trends

Rep-Lite

As the healthcare landscape continues to evolve, so too does the role of medical device specialists. At Rep-Lite, we understand the importance of staying ahead of industry trends to support medical device sales recruiting effectively and foster the growth of tomorrow’s professionals.

Medical 52