CLINICAL TRIAL PATIENT TECHNOLOGY INSIGHTS
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![Tablets, smartphones-GettyImages-910535708]( "Ask An Expert Before Shredding Your Mobile Device CAPEX")
Ask An Expert Before Shredding Your Mobile Device CAPEXTasked with buying your company's mobile devices and not sure where to start? Discover the questions you should ask and the information you need to know before consulting an expert.
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![consultation, examination result, electronic prescription-GettyImages-1403523137]( "Paving The Way For Sites To Use Their Own Tech")
Paving The Way For Sites To Use Their Own TechThe DTRA has released a detailed playbook to help clinical research sites use their own validated technology in sponsor-led trials. The "Bring Your Own Technology" (BYOT) model aims to reduce tech overload at sites, improve efficiency, and preserve regulatory compliance — starting with eConsent as its first use case.
ECOA RESOURCES
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![Doctor Using Digital Tablet GettyImages-1530254515]( "Addressing The Challenges Of eCOA Licensing")
How can you combat the instrument licensing and linguistic validation challenges associated with adopting electronic Clinical Outcome Assessments (eCOA), ensuring quick access to source files?
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![Navigate A Path]( "Taking eCOA Technology Deployment Off The Critical Path")
Consider this expedited review approach to facilitate the efficient evaluation of COAs and eCOAs, streamlining the pathway for successful trial execution.
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The shift from reporting on paper to reporting electronically has been happening for years, however, the transition hasn’t always been elegant. Explore how the pandemic has played a role in accelerating the shift to eCOA/ePRO.
ECONSENT RESOURCES
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![Can Electronic Health Records Bring Down Drug Prices?]( "Protocol Amendments And Electronic Consent: Overcoming The Challenges To Reap The Benefits")
Learn about some insights that have been gleaned from experience deploying eConsent on diverse trial types around the world.
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![The New Era Of Evidence Generation In Clinical Trials]( "The New Era Of Evidence Generation In Clinical Trials")
Learn how top pharmaceutical companies are using novel innovations to drive greater speed, scale, and access in clinical research than ever before in this webinar hosted by Musaddiq Khan, Vice President of DCT Solutions at Medable.
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![GettyImages-1295492925-computer-future-data-research-lab]( "Headed Down Registry Road? Here Are The EDC Features You'll Need")
Most of us rely on electronic data capture (EDC) to help us reach our study destination. How do we choose the EDC "vehicle" that will get us there safely, with minimal delays? Consider the relative importance of these key EDC features.
EPRO RESOURCES
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![Clinical Trials Electronic Informed Consent: ePRO, EDC, eTMF]( "Could ePRO Be The New Standard In Health Reimbursement?")
Recently, early-phase protocols have been collecting patient-reported outcomes (PROs) not only to get regulatory approval but to demonstrate value to public and private payers.
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The shift from reporting on paper to reporting electronically has been happening for years, however, the transition hasn’t always been elegant. Explore how the pandemic has played a role in accelerating the shift to eCOA/ePRO.
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![eCOA Resources Overview]( "C3 Summit Recap: Shaping The Future Of eCOA/ePRO Highlights")
Understand how the rapid shift to decentralized clinical trials required pharma companies and CROs to adapt data capture techniques quickly while remaining compliant with local regulations.
