Discover where the bottlenecks are in your #ClinicalTrial with graphical reports that are auto-generated from the study's workflow -- w/ no programming & no extra cost! See our CTO's post, "Managing complex clinical trials," https://t.co/Tmmaqk8RKi
#Clinpal
A #ClinicalTrial can have #VirtualTrial components included w/ a rapid setup & deployment on iOS & Android smartphones and PC & Mac browsers. Watch the #Clinpal webinar free on demand at https://t.co/QjNuichbYt
Read our CTO's blog post released today at https://t.co/NnjizVDWxd. @wdougbain discusses the emerging field of #DigitalHealth in a blog post about #ClinicalTrials employing medical apps.
If you registered for the #Clinpal webinar -- Virtual Clinical Trial of Digital Therapy App in Depression -- now is the time to click the link you received by email to sign in. The webinar begins in 15 minutes at 10 EDT, 3 BST.
Sign up now for tomorrow's #Clinpal webinar describing the rapid setup & deployment of an #RCT#VirtualClinicalTrial in #depression supporting @meruhealth's smartphone app which delivers a remote online #DigitalTherapy program. https://t.co/3GMdjw80H9 11 SEP at 10AM EDT, 3PM BST.
Learn about the #VirtualClinicalTrial@meruhealth is delivering via a smartphone app supported by mental health professionals, with the #Clinpal platform for #RemoteResearch. Register for the webinar on 11th September at 10:00 New York/15:00 London. https://t.co/3GMdjw80H9
Enrolling qualified study participants is hard. But getting them to stay in studies can be even harder. See how Merge Clinical Study Communications does it.
https://t.co/lDlSfGtZBo
After #Clinpal#eConsent records a patient's + investigator's #eSignature, Clinpal allows patients to be enrolled, randomized, reminded, & questioned using the same platform with all data, forms, histories tracked in one location with role-based views across the data.
#Clinpal includes the appropriate workflow to notify a site or investigator that he or she needs to co-sign an #eConsent form and provides an #ElectronicSignature process. Learn more about Clinpal eConsent solution at https://t.co/vXwbT1dQYF
#Clinpal includes #ElectronicSignatures to facilitate the signing process for #eConsent. Once signed, the #InformedConsent form can be printed by the patient or by site staff. Learn more in the explainer video: https://t.co/7XH4SioU9O
#Clinpal#eConsent alerts sites when an updated version of the #InformedConsent is published and subjects must be re-consented. Subjects have access to only the current approved version of the consent forms. Read more about Clinpal's eConsent solution at https://t.co/vXwbT1dQYF
#Clinpal can include knowledge assessments or quizzes to measure subject comprehension after reading the #eConsent form and viewing the video. https://t.co/7XH4SioU9O Contact us to learn more about the Clinpal platform for clinical trials at https://t.co/4fR2anSErq
#Clinpal manages changes to the #eConsent form by site or region depending on the IRB/EC approvals, significantly reducing chance of error & providing immediate global access to the most up-to-date versions. Learn more in the explainer video: https://t.co/7XH4SioU9O
#Clinpal can manage multiple #InformedConsent versions based on study needs (by state, age group, language, country, or other criteria) using the necessary dynamic logic to present the right #eConsent to the right subject. https://t.co/vXwbT1dQYF
#Clinpal#eConsent improves many aspects of the #InformedConsent process by providing an online learning tool that centralizes and controls the process, with the consent information presented in a standardized way for every site. https://t.co/vXwbT1dQYF
#Clinpal#eConsent improves the accuracy of the consent process by reducing versioning errors and distribution problems. This type of error is the primary source of audit findings according to FDA inspection data (FDA BIMO Inspection Report, 2014). https://t.co/vXwbT1dQYF