CLINICAL TRIAL PATIENT TECHNOLOGY INSIGHTS
-
DiMe's Navigator: Why Teams Still Stall On Digital Endpoints
DiMe’s sDHT Adoption Navigator helps clinical teams move from guidance to action, but the real test is whether organizations use it early enough to matter.
-
Digital Endpoints Are Ready. Clinical Development Isn't
Regulatory guidance and validation science for digital endpoints are solid. The real barrier is cross-functional execution – and the cost of waiting is compounding.
ECOA RESOURCES
-
Unearth the innovative ways electronic clinical outcome assessments (eCOA) are improving data accuracy, reducing errors, and ensuring robust oversight in clinical trials.
-
Uncover how a top-10 pharmaceutical company was able to overcome oncology clinical study obstacles with a digital software platform.
-
The solution to administrative burden in clinical trials is not in adding more tools, but in improved integration that allows software to fade into the background.
ECONSENT RESOURCES
-
Watch this webinar to see the latest eConsent workflow from recruitment, to pre-screening, to remote consent.
-
Learn the distinctions between a Waiver of Consent and a Waiver of Written Consent in clinical trials, and the importance of informed consent, particularly in the context of virtual trials.
-
Learn how eConsent digitalizes the trial participant consent process through increasingly simplified models designed to improve comprehension and boost engagement.
EPRO RESOURCES
-
If you are in the early stages of an oncology trial, there is a lot to consider when it comes to your data management and how the process can be simplified by improving how your study captures data.
-
Learn how eConsent digitalizes the trial participant consent process through increasingly simplified models designed to improve comprehension and boost engagement.
-
Unearth how this global eClinical provider delivered a decentralized platform including eSource/ePRO for direct-data-entry, randomization, eConsent, telehealth, remote monitoring, and data management.