Medical device companies rely on data that validates the efficacy of the device, proves its quality, and demonstrates satisfaction. Excluding PROs from that dataset limits a product’s success. ResearchPRO was designed to make data collection cost-effective for medical device companies of all sizes. Learn more here: https://bit.ly/3PCpEdM
PatientIQ的动态
最相关的动态
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Discover how Interactive Response Technology (IRT) is transforming medical device trials! By reducing costs and streamlining processes, IRT accelerates time-to-market, ensuring devices reach patients efficiently. Learn more about our solution in the latest Medical Product Outsourcing article by Kevin Landells: https://bit.ly/4fHEqL6
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New Blog: "The Path to Launching a Medical Device in the USA: A Guide by OneGlobal Trinity M Consulting." Read more below. https://wix.to/QbUicbZ #trinitymconsulting #globalconsulting #medicaldevices #newblogpost
The Path to Launching a Medical Device in the USA: A Guide by OneGlobal Trinity M Consulting
trinitymconsulting.com
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There are about 2 million medical devices on the market today, and each of them underwent a journey from innovation through clinical trials to the market. The journey might look familiar, but medical device trials come with particular challenges. Here we look at what they are and how to overcome them. https://buff.ly/3LZePS0 #MedicalDevice #ClinicalTrials #ClinicalResearch
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What does the future look like for medical device transit? Christopher Mills and Bradley Lethby evaluate the considerations in a clip from our webinar: 'Transit Testing for Medical Device Packaging'. Click here to watch the webinar in full on demand: https://lnkd.in/eh9VDYSb
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Why is task analysis crucial in medical device development? Learn the top 3 reasons why in our latest blog, the first of a five-article series. Tap into the knowledge from two of our Human Factors experts and take the first step towards minimizing use-related risks: https://bit.ly/3VP84aj #humanfactors #medicaldevices #userexperience #taskanalysis #designthinking #healthcareinnovation #FDAregulations #productdevelopment
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Helping Ambitious Leaders Achieve Product Development Success Through Informed Design?
Why is task analysis crucial in medical device development? Learn the top 3 reasons why in our latest blog, the first of a five-article series. Tap into the knowledge from two of our Human Factors experts and take the first step towards minimizing use-related risks: https://bit.ly/3JaIqp9 #humanfactors #medicaldevices #userexperience #taskanalysis #designthinking #healthcareinnovation #FDAregulations #productdevelopment
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** Newest Blog Post ** Top 5 Regulatory Trends in the Advanced Medical Device Industry A Link to the Article: https://lnkd.in/gfgMgstn
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Clinical & Regulatory Affairs Director @ CLIN-r+ | International lead - Medical Device Regulation (MDR) support
SLR’s is a systemic process that needs to produce repeatable results. And it need good curated databases that provide consistent outputs. See their podcast or our white papers for insights: https://lnkd.in/d2S4xTgq https://lnkd.in/dtH3Upr8
What does a compliant systematic literature review for medical devices look like? From screening for bias to levels of evidence, get access to rich insights within this recorded webinar and other resources on medical device regulation. https://spkl.io/6048f8zBp #EUMDR #MedicalDevices
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Why is task analysis crucial in medical device development? Learn the top 3 reasons why in our latest blog, the first of a five-article series. Tap into the knowledge from two of our Human Factors experts and take the first step towards minimizing use-related risks: https://bit.ly/4cROLn2 #humanfactors #medicaldevices #userexperience #taskanalysis #designthinking #healthcareinnovation #FDAregulations #productdevelopment
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Learn about our authentic analytics strategies that drove informed decisions in the medical device industry. 30-min Deminar ( Demo + Webinar ) on “Modernizing Data to Decisions for Medical Device Manufacturers.” Register here: https://lnkd.in/gG9ntwWQ #gaininsights #medicaldevices #analytics
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