Medable: Decentralized clinical trials platform.

But it wasn’t until Covid became popular that all of those other world embraced Longmire’s perspective on the importance of technology in raising these figures.
Medable’s Decentralized Clinical Trial platform is the industry’s first digital clinical trial platform that improves research by enabling every biology to easily take part in trials all over the world while driving precise outcomes and scaling to match the needs of any protocol.
Medable recently launched a software solution to shorten the launch times for decentralized vaccine trials.
The company says the program can reduce trial deployment timelines from a lot more than 12 weeks normally to as short as five weeks.

Through the implementation of direct-to-patient healthcare, it improves clinical care and research by providing an end-to-end, cloud-based platform with a customizable suite of tools for clinical trials.
The business enterprise offers remote patient monitoring, vaccine options, digital and direct Coombs test screening, among other services.
Through this decentralized clinical trials, GSK aims to increase access to research, improve diversity and create more patient-centric trial designs.
Clinical trial models are evolving rapidly, allowing us to offer you new approaches that may increase patient recruitment, and engagement and retention, and promote continuity for your clinical trial.

For Phase III studies, similar deployment time savings can yield a net benefit that is up to 13 times greater than the required upfront investment.
The rate of innovation in vaccine research was pretty low before pandemic emerged, according to Khan.
Now that scientific innovation is taking off in the vaccine space (think mRNA technology found in Pfizer and Moderna’s Covid-19 vaccines), it is time for operational delivery to modernize aswell, he argued.

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Explore an expertly crafted package of programs, products, and expertise addressing the unique challenges of vaccine research.
Understand how drug makers worldwide must ensure that conditions for bias aren’t created as a result of usage of devices or WiFi when it comes to clinical research.
Last month, Medable announced that its software as a service electronic management solution, Total Consent​, was available at more than 120 locations worldwide.
For these DCTs, GSK selected Medable’s end-to-end DCT platform that provides several digital capabilities including TeleVisit, eConsent, and eCOA.

Based on the American Medical Association, while 85% of individuals claim they want to engage in research, significantly less than 5% of eligible patients actually do, and racial minorities are routinely underrepresented.
Study released earlier this season by the Tufts Center for the analysis of Drug Development said that for decentralized Phase II studies, the one to three month reduction in deployment time yields a net financial benefit that’s around five times higher than the upfront investment required.

• Read this blog to learn more about how eConsent can enhance participant engagement and retention when used both onsite and remotely.
• Hear from skillfully developed on what they successfully combined agile eConsent technology with global regulatory expertise to increase enrollment rates and reduce both site and patient burden.
• Traveling to a niche site is one of the primary obstacles to participation, therefore Medable helps it be easier for pharmaceutical companies to attract and keep a wider selection of participants.
• Its growth of 300% on the previous year and more than 800% on the previous 18 months, according to Longmire, this is the evidence that a patient-centered approach is beginning to catch on.

This “off-the-shelf solution” eliminates much of the technical build burden for pharmaceutical companies and may reduce trial launch timelines from more than 12 weeks normally to as short as five weeks, Khan claimed.
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In this webinar, Medable SMEs take you through the end-to-end procedure for conducting decentralized clinical research, including benefits, common pitfalls and challenges, and much more.
In this on-demand webinar attendees will learn about the common misconceptions surrounding eConsent, as well as the benefits they are able to realize through a digitally-enabled approach.

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According to Digital Health Business & Technology’s database, the amount of decentralized clinical technology companies receiving funding has increased each of the last three quarters.
Discover how Medable has developed a business first certification program made to provide your workforce with the specialized tools, knowledge, and skills essential to rapidly scale decentralized and hybrid trials.

“This dynamic collaboration with Medable can help us intensify our efforts to operate a vehicle meaningful awareness and usage of a broader population, in particular those with mounting chronic illnesses and the vulnerable populations who today are underrepresented in clinical research.
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Carrying out a thorough assessment of top clinical trial platforms, Medable’s technology was selected because it best supports the goals of GSK for boosting access to research, diversity, and making trial designs that are more patient centred.
Less than 4% of Americans take part in clinical trials; 30% drop out before the end of the analysis; and 80% neglect to reach enrollment targets.

Medable and Syneos Health first partnered in April 2021 and also have since collaborated on a lot more than fifteen clinical trials across multiple therapeutic areas.
Since the beginning of their partnership, Syneos Health insurance and Medable, had adopted tools to create a scalable operational model for decentralized and hybrid studies.
Its growth of 300% on the previous year and much more than 800% on the previous 18 months, according to Longmire, this is the evidence that a patient-centered approach is starting to catch on.
The company’s software has impacted the lives of thousands of patients and is being used in 150 clinical trials which are being conducted at 5,000 clinical sites in 60 countries.
Medable Inc. today announced a multi-company research framework to accelerate development of diagnostics and treatments for COVID-19, providing individuals fast access to take part in leading-edge research for diagnostics, health monitoring and interventional clinical trials.
We modernize clinical research with solutions such as for example digital recruitment, patient engagement, eConsent, eCOA, telehealth virtual visits, site data capture, sensors and analytics.