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By Dan Schell, chief editor, Clinical Leader | Bari Kowal, SVP of development operations, portfolio management & biostatistics data management at Regeneron, reveals that the industry is just scratching the surface of digital biomarker benefits, highlighting the challenge of identifying reliable, repeatable measurements. |
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| 3 Things To Know When Using Wearables In Your Study | Article | By Kristen Harnack, Castor | As wearables unleash new possibilities, the industry will need an effective strategy to utilize these useful tools. Consider these tips when incorporating wearables in a clinical study. |
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| Why Your eTMF Needs Role-Based Access | Article | Anju Software | Discover how role-based access controls can offer a way for clinical teams to answer the tough questions from regulators, investors, and other parties. |
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| 7 eCOA Design Recommendations: Insights From Sites And CRAs | Article | By Katie Garner, Signant Health | Signant joined a group of C-Path members including other eCOA solution providers, sponsors, and regulators for a GBTI project that revealed several opportunities to improve eCOA usability and flexibility. |
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| Right-Size Your eConsent Approach | Webinar | IQVIA Technologies | Learn to tailor the eConsent experience to match your study's and patients' specific needs, such as crafting patient-centric eConsent documents, selecting appropriate delivery, and more. |
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| Patient Perspectives On eConsent | White Paper | Medidata, a Dassault Systemes company | Delve into how eConsent enables participants to engage meaningfully with consent documentation, addressing information dissemination, explanation, and recall challenges. |
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| Driving ROI Through Patient Convenience Solutions | White Paper | Greenphire | Uncover the findings from this third-party ROI analysis firm that conducted interviews with customers to assess their experiences using Greenphire's Participant Reimbursement and Travel Solutions. |
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