eConsent Saves Time And Increases Patient Engagement In Clinical Trial Startup

Clinical Ink’s eConsent module is an all-in-one solution that optimizes your consent process for simpler study startup. Not only does it reduce site workload, saving you time and money, but it delivers a better patient experience. The eConsent module can stand alone or be deployed within our Lumenis platform, an integrated, convenient eSource solution that includes additional modules such as ePRO and eCOA. Lumenis eases study conduct for both study teams and sites, improves data quality, and supports clear and confident decision-making.

Key Benefits

• Optimize the Patient Experience
• Improve Your Consent Process
• Reduce Site Workload; Save Time and Money