In this webinar, experts from ObvioHealth, Oracle, and PPD provide key insights for driving operational efficiencies and successfully streamlining multisource data sets into a consolidated and actionable source of truth—all to remove burden from the clinical continuum and deliver tomorrow’s powerful insights.
With the emergence of decentralized clinical trials, we now have a window into patients’ clinical trial experiences like never before. Not only are we collecting more, and arguably better, data through real-world direct patient reporting, but data is also coming from a broader range of sources, including sites, labs, devices, CROs, EHRs, and RWD. This greater access provides us with new, more accurate ways to measure outcomes—and unlocks previously unobtainable insights.
The ultimate goal of using digital and decentralized research methods is to remove burden from the entire clinical continuum. But, while hybrid study designs might, on one hand, make patient participation easier, new pain points have simultaneously been introduced for study administrators and clinicians.
How do we ensure sponsors, sites, and study teams can efficiently and easily manage this wealth of new data to deliver actionable insights? And, how can we streamline complex data sets into a single and actionable source of truth?
Listen in as our experts explore these questions and more, including:
· How to operationalize decentralized clinical trial study designs.
· How innovative data capture methods (e.g., sensors and wearables) can improve the quality of patient data.
· How to solve operational headaches at sites with streamlined workflows to ease reporting and data management.
· How the magnitude and multi-source nature of data captured in today’s decentralized trials requires systems capable of aggregating and integrating to provide a single source of truth.
· How innovative trial designs can be offered at scale now to drive operational efficiencies, deliver tomorrow’s powerful insights, and remove burden from the clinical continuum.
In thiswebinar, experts from ObvioHealth, Oracle, and PPD provide key insights fordriving operational efficiencies and successfully streamlining multisource datasets into a consolidated and actionable source of truth—all to remove burdenfrom the clinical continuum and deliver tomorrow’s powerful insights.
With the emergence of decentralized clinical trials, we now have a window into patients’ clinical trial experiences like never before. Not only are we collecting more, and arguably better, data through real-world direct patient reporting, but data is also coming from a broader range of sources, including sites, labs, devices, CROs, EHRs, and RWD. This greater access provides us with new, more accurate ways to measure outcomes—and unlocks previously unobtainable insights.
The ultimate goal of using digital and decentralized research methods is to remove burden from the entire clinical continuum. But, while hybrid study designs might, on one hand, make patient participation easier, new pain points have simultaneously been introduced for study administrators and clinicians.
How do we ensure sponsors, sites, and study teams can efficiently and easily manage this wealth of new data to deliver actionable insights? And, how can we streamline complex data sets into a single and actionable source of truth?
Listen in as our experts explore these questions and more, including:
· How to operationalize decentralized clinical trial study designs.
· How innovative data capture methods (e.g., sensors and wearables) can improve the quality of patient data.
· How to solve operational headaches at sites with streamlined workflows to ease reporting and data management.
· How the magnitude and multi-source nature of data captured in today’s decentralized trials requires systems capable of aggregating and integrating to provide a single source of truth.
· How innovative trial designs can be offered at scale now to drive operational efficiencies, deliver tomorrow’s powerful insights, and remove burden from the clinical continuum.
In this webinar, experts from ObvioHealth, Oracle, and PPD provide key insights for driving operational efficiencies and successfully streamlining multisource data sets into a consolidated and actionable source of truth—all to remove burden from the clinical continuum and deliver tomorrow’s powerful insights.
With the emergence of decentralized clinical trials, we now have a window into patients’ clinical trial experiences like never before. Not only are we collecting more, and arguably better, data through real-world direct patient reporting, but data is also coming from a broader range of sources, including sites, labs, devices, CROs, EHRs, and RWD. This greater access provides us with new, more accurate ways to measure outcomes—and unlocks previously unobtainable insights.
The ultimate goal of using digital and decentralized research methods is to remove burden from the entire clinical continuum. But, while hybrid study designs might, on one hand, make patient participation easier, new pain points have simultaneously been introduced for study administrators and clinicians.
How do we ensure sponsors, sites, and study teams can efficiently and easily manage this wealth of new data to deliver actionable insights? And, how can we streamline complex data sets into a single and actionable source of truth?
Listen in as our experts explore these questions and more, including:
· How to operationalize decentralized clinical trial study designs.
· How innovative data capture methods (e.g., sensors and wearables) can improve the quality of patient data.
· How to solve operational headaches at sites with streamlined workflows to ease reporting and data management.
· How the magnitude and multi-source nature of data captured in today’s decentralized trials requires systems capable of aggregating and integrating to provide a single source of truth.
· How innovative trial designs can be offered at scale now to drive operational efficiencies, deliver tomorrow’s powerful insights, and remove burden from the clinical continuum.
With the emergence of decentralized clinical trials, we now have a window into patients’ clinical trial experiences like never before. Not only are we collecting more, and arguably better, data through real-world direct patient reporting, but data is also coming from a broader range of sources, including sites, labs, devices, CROs, EHRs, and RWD. This greater access provides us with new, more accurate ways to measure outcomes—and unlocks previously unobtainable insights.
The ultimate goal of using digital and decentralized research methods is to remove burden from the entire clinical continuum. But, while hybrid study designs might, on one hand, make patient participation easier, new pain points have simultaneously been introduced for study administrators and clinicians.
How do we ensure sponsors, sites, and study teams can efficiently and easily manage this wealth of new data to deliver actionable insights? And, how can we streamline complex data sets into a single and actionable source of truth?
Listen in as our experts explore these questions and more, including:
· How to operationalize decentralized clinical trial study designs.
· How innovative data capture methods (e.g., sensors and wearables) can improve the quality of patient data.
· How to solve operational headaches at sites with streamlined workflows to ease reporting and data management.
· How the magnitude and multi-source nature of data captured in today’s decentralized trials requires systems capable of aggregating and integrating to provide a single source of truth.
· How innovative trial designs can be offered at scale now to drive operational efficiencies, deliver tomorrow’s powerful insights, and remove burden from the clinical continuum.
With the emergence of decentralized clinical trials, we now have a window into patients’ clinical trial experiences like never before. Not only are we collecting more, and arguably better, data through real-world direct patient reporting, but data is also coming from a broader range of sources, including sites, labs, devices, CROs, EHRs, and RWD. This greater access provides us with new, more accurate ways to measure outcomes—and unlocks previously unobtainable insights.
The ultimate goal of using digital and decentralized research methods is to remove burden from the entire clinical continuum. But, while hybrid study designs might, on one hand, make patient participation easier, new pain points have simultaneously been introduced for study administrators and clinicians.
How do we ensure sponsors, sites, and study teams can efficiently and easily manage this wealth of new data to deliver actionable insights? And, how can we streamline complex data sets into a single and actionable source of truth?
Listen in as our experts explore these questions and more, including:
· How to operationalize decentralized clinical trial study designs.
· How innovative data capture methods (e.g., sensors and wearables) can improve the quality of patient data.
· How to solve operational headaches at sites with streamlined workflows to ease reporting and data management.
· How the magnitude and multi-source nature of data captured in today’s decentralized trials requires systems capable of aggregating and integrating to provide a single source of truth.
· How innovative trial designs can be offered at scale now to drive operational efficiencies, deliver tomorrow’s powerful insights, and remove burden from the clinical continuum.
In this webinar, experts from ObvioHealth, Oracle, and PPD provide key insights for driving operational efficiencies and successfully streamlining multisource data sets into a consolidated and actionable source of truth—all to remove burden from the clinical continuum and deliver tomorrow’s powerful insights.
With the emergence of decentralized clinical trials, we now have a window into patients’ clinical trial experiences like never before. Not only are we collecting more, and arguably better, data through real-world direct patient reporting, but data is also coming from a broader range of sources, including sites, labs, devices, CROs, EHRs, and RWD. This greater access provides us with new, more accurate ways to measure outcomes—and unlocks previously unobtainable insights.
The ultimate goal of using digital and decentralized research methods is to remove burden from the entire clinical continuum. But, while hybrid study designs might, on one hand, make patient participation easier, new pain points have simultaneously been introduced for study administrators and clinicians.
How do we ensure sponsors, sites, and study teams can efficiently and easily manage this wealth of new data to deliver actionable insights? And, how can we streamline complex data sets into a single and actionable source of truth?
Listen in as our experts explore these questions and more, including:
· How to operationalize decentralized clinical trial study designs.
· How innovative data capture methods (e.g., sensors and wearables) can improve the quality of patient data.
· How to solve operational headaches at sites with streamlined workflows to ease reporting and data management.
· How the magnitude and multi-source nature of data captured in today’s decentralized trials requires systems capable of aggregating and integrating to provide a single source of truth.
· How innovative trial designs can be offered at scale now to drive operational efficiencies, deliver tomorrow’s powerful insights, and remove burden from the clinical continuum.
In this webinar, experts from ObvioHealth, Oracle, and PPD provide key insights for driving operational efficiencies and successfully streamlining multisource data sets into a consolidated and actionable source of truth—all to remove burden from the clinical continuum and deliver tomorrow’s powerful insights.
With the emergence of decentralized clinical trials, we now have a window into patients’ clinical trial experiences like never before. Not only are we collecting more, and arguably better, data through real-world direct patient reporting, but data is also coming from a broader range of sources, including sites, labs, devices, CROs, EHRs, and RWD. This greater access provides us with new, more accurate ways to measure outcomes—and unlocks previously unobtainable insights.
The ultimate goal of using digital and decentralized research methods is to remove burden from the entire clinical continuum. But, while hybrid study designs might, on one hand, make patient participation easier, new pain points have simultaneously been introduced for study administrators and clinicians.
How do we ensure sponsors, sites, and study teams can efficiently and easily manage this wealth of new data to deliver actionable insights? And, how can we streamline complex data sets into a single and actionable source of truth?
Listen in as our experts explore these questions and more, including:
· How to operationalize decentralized clinical trial study designs.
· How innovative data capture methods (e.g., sensors and wearables) can improve the quality of patient data.
· How to solve operational headaches at sites with streamlined workflows to ease reporting and data management.
· How the magnitude and multi-source nature of data captured in today’s decentralized trials requires systems capable of aggregating and integrating to provide a single source of truth.
· How innovative trial designs can be offered at scale now to drive operational efficiencies, deliver tomorrow’s powerful insights, and remove burden from the clinical continuum.
In this webinar, our expert panelists—including a participant—explore the Mi-Helper clinical trial as a case study, reviewing the challenges associated with conducting medical device studies remotely, and how collaboration and iteration can help to identify and mitigate risks from the outset. Download the webinar summary by filling out the form below.
In this webinar, our expert panelists address the challenges and opportunities associated with sensors and wearables in clinical research—and how sponsors and study teams can incorporate these instruments to maximize the signal-to-noise ratio, increase patient comfort, and generate stronger, more robust evidence. Download the webinar summary and key takeaways in PDF format by filling out the form below.