Patient Data Reporting Videos
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Discover Curebase: End-To-End Clinical Trial Execution Built On Cutting-Edge Technology
6/28/2022
In this video, learn more about the full-service clinical trial management, virtual and hybrid sites, and comprehensive eClinical software platform that Curebase offers.
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Get Your TMF Health Score
5/11/2022
Introducing the TMF Health Score – an expert methodology that provides an “early warning system” to commonly overlooked issues that often lead to inspection findings.
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Fast, Flexible, And Proven Direct-From-Patient Data Capture With eCOA
5/3/2022
Delve into how IQVIA eCOA captures patient data in a way that always keeps patients top of mind.
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Mobile Assessments For Parkinson's Disease Research
3/30/2022
In this video, see firsthand fit-for-purpose mobile assessments and applications designed to measure endpoints in Parkinson’s Disease.
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Biocon's Rashika Suri Improves Approach To Managing Trial Master Files
3/7/2022
Biocon is India’s largest biopharmaceutical company and an early adopter of the LifeSphere eTMF system. Rashika Suri, Head of Clinical Quality and Compliance at Biocon, discusses the importance of collaboration when implementing new technology.
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ArisGlobal BREAKTHROUGH: LifeSphere CTMS, eTMF, And EDC
3/4/2022
Learn more about LifeSphere CTMS, eTMF, and EDC – highlighted in this video from ArisGlobal’s annual customer event, BREAKTHROUGH.
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eTMF For Clinical Trial Master Files And Operations
3/2/2022
This video shows how a modern eTMF system built with a new exchange standard promises to bring better collaboration and compliance.
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Electronic Data Capture (EDC) System For Clinical Research Trials
2/7/2022
Reduce time spent on building and managing studies. Be it single center or multicenter studies, Castor EDC’s user-friendly form builder, advanced user management and workflow will streamline your data capture for all your clinical trials.
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Key #5 For Successful ePRO Selection In Your Ophthalmology Clinical Trial: Anticipate Cultural Differences In Multi Country Clinical Trials
11/3/2021
Before selecting a PRO for use in a large global trial, it is important to anticipate that responses to questionnaires may vary based on the country or cultural differences. Watch the available video to see how good preparation and planning can help with finding a balance between maintaining cultural relevance and data quality.
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Key #4 For Successful ePRO Selection In Your Ophthalmology Clinical Trial: Consider The Method Of ePRO Administration
11/2/2021
PROs in ophthalmology trials can either be self-administered by the patient or the responses can be collected through an interview, administered by the investigator or site personnel. They both present advantages and drawbacks that can affect the responses provided by the patients.