The purpose of an IRB is to assure that appropriate steps are taken to protect the rights and welfare of humans participating as subjects in the research. Putting the patient first in clinical trials is a grounding value we must never stray from. At Curebase, we believe it is important to seek advice and understanding proactively from those that represent the patient's best interest. As technology advances in clinical research, the rights of the patients must be at the forefront of our minds, as naturally technologists may get caught up in their own inventions and stray from the original goals of better serving the patient. We’ve built Curebase from the ground up with this in mind, as we move decentralized clinical trials forward into new areas of research.
To gain insight into the considerations and position of the IRB on decentralization of clinical studies, our CEO Tom Lemberg sat down with the President of IntegReview IRB, Melanie Flores, to discuss. In this webinar, Melanie shares from her 20+ years of experience how the perspectives and considerations for decentralized clinical trials have evolved, and what to consider for future studies, as technology progresses, in protecting patient’s rights.
About Curebase
Curebase is reinventing decentralized clinical trials to help the vast majority of potential patients that currently cannot access clinical research. Our vision is that any patient, no matter where they are located, should be able to participate in clinical trials at home and with their own doctors. This is made possible through a unique suite of tools Curebase’s has designed to engage patients in clinical trials across all settings, be it at home, at their local clinic, or other places in their community.
This starts with Curebase’s leading decentralized clinical trial software platform that is an all-in-one, purpose built eClinical software system, with every tool needed to manage and collect data for decentralized clinical trials. This includes ePRO, eCOA, eConsent, Telemedicine, and much more. Curebase also offers a virtual research site, complete with virtual investigators, research coordinators, mobile nursing, and other healthcare staff that administer care to patients where convenient for them, just like any other research site, but with the ability to stand up anywhere and with greater patient convenience and reach. Notably, Curebase is the pioneer of the “BYOP” or Bring Your Own Physician model, allowing patients to use their own doctors to participate in clinical trials.
We are reinventing a $45B market, enabling drug and device companies to increase the volume, quality, and speed of data collection regardless of patients’ physical location. COVID-19 tailwinds have created massive demand for telemedicine and home-based trials, with two new FDA guidance letters and industry-wide adoption of remote remote research that will only accelerate in the years to come. You can learn more about Curebase and our next stage of growth in Crunchbase, Fierce Biotech, and MedCity News!
Interested in staying up to date with Curebase's latest developments in the decentralized clinical trial space? Get regular updates on news, webinars, blogs and more by subscribing here.
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The purpose of an IRB is to assure that appropriate steps are taken to protect the rights and welfare of humans participating as subjects in the research. Putting the patient first in clinical trials is a grounding value we must never stray from. At Curebase, we believe it is important to seek advice and understanding proactively from those that represent the patient's best interest. As technology advances in clinical research, the rights of the patients must be at the forefront of our minds, as naturally technologists may get caught up in their own inventions and stray from the original goals of better serving the patient. We’ve built Curebase from the ground up with this in mind, as we move decentralized clinical trials forward into new areas of research.
To gain insight into the considerations and position of the IRB on decentralization of clinical studies, our CEO Tom Lemberg sat down with the President of IntegReview IRB, Melanie Flores, to discuss. In this webinar, Melanie shares from her 20+ years of experience how the perspectives and considerations for decentralized clinical trials have evolved, and what to consider for future studies, as technology progresses, in protecting patient’s rights.
About Curebase
Curebase is reinventing decentralized clinical trials to help the vast majority of potential patients that currently cannot access clinical research. Our vision is that any patient, no matter where they are located, should be able to participate in clinical trials at home and with their own doctors. This is made possible through a unique suite of tools Curebase’s has designed to engage patients in clinical trials across all settings, be it at home, at their local clinic, or other places in their community.
This starts with Curebase’s leading decentralized clinical trial software platform that is an all-in-one, purpose built eClinical software system, with every tool needed to manage and collect data for decentralized clinical trials. This includes ePRO, eCOA, eConsent, Telemedicine, and much more. Curebase also offers a virtual research site, complete with virtual investigators, research coordinators, mobile nursing, and other healthcare staff that administer care to patients where convenient for them, just like any other research site, but with the ability to stand up anywhere and with greater patient convenience and reach. Notably, Curebase is the pioneer of the “BYOP” or Bring Your Own Physician model, allowing patients to use their own doctors to participate in clinical trials.
We are reinventing a $45B market, enabling drug and device companies to increase the volume, quality, and speed of data collection regardless of patients’ physical location. COVID-19 tailwinds have created massive demand for telemedicine and home-based trials, with two new FDA guidance letters and industry-wide adoption of remote remote research that will only accelerate in the years to come. You can learn more about Curebase and our next stage of growth in Crunchbase, Fierce Biotech, and MedCity News!
The purpose of an IRB is to assure that appropriate steps are taken to protect the rights and welfare of humans participating as subjects in the research. Putting the patient first in clinical trials is a grounding value we must never stray from. At Curebase, we believe it is important to seek advice and understanding proactively from those that represent the patient's best interest. As technology advances in clinical research, the rights of the patients must be at the forefront of our minds, as naturally technologists may get caught up in their own inventions and stray from the original goals of better serving the patient. We’ve built Curebase from the ground up with this in mind, as we move decentralized clinical trials forward into new areas of research.
To gain insight into the considerations and position of the IRB on decentralization of clinical studies, our CEO Tom Lemberg sat down with the President of IntegReview IRB, Melanie Flores, to discuss. In this webinar, Melanie shares from her 20+ years of experience how the perspectives and considerations for decentralized clinical trials have evolved, and what to consider for future studies, as technology progresses, in protecting patient’s rights.
About Curebase
Curebase is reinventing decentralized clinical trials to help the vast majority of potential patients that currently cannot access clinical research. Our vision is that any patient, no matter where they are located, should be able to participate in clinical trials at home and with their own doctors. This is made possible through a unique suite of tools Curebase’s has designed to engage patients in clinical trials across all settings, be it at home, at their local clinic, or other places in their community.
This starts with Curebase’s leading decentralized clinical trial software platform that is an all-in-one, purpose built eClinical software system, with every tool needed to manage and collect data for decentralized clinical trials. This includes ePRO, eCOA, eConsent, Telemedicine, and much more. Curebase also offers a virtual research site, complete with virtual investigators, research coordinators, mobile nursing, and other healthcare staff that administer care to patients where convenient for them, just like any other research site, but with the ability to stand up anywhere and with greater patient convenience and reach. Notably, Curebase is the pioneer of the “BYOP” or Bring Your Own Physician model, allowing patients to use their own doctors to participate in clinical trials.
We are reinventing a $45B market, enabling drug and device companies to increase the volume, quality, and speed of data collection regardless of patients’ physical location. COVID-19 tailwinds have created massive demand for telemedicine and home-based trials, with two new FDA guidance letters and industry-wide adoption of remote remote research that will only accelerate in the years to come. You can learn more about Curebase and our next stage of growth in Crunchbase, Fierce Biotech, and MedCity News!
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Interested in staying up to date with Curebase's latest developments in the decentralized clinical trial space? Get regular updates on news, webinars, blogs and more by subscribing here.
