Modern Clinical trials have undergone a huge shift in the need for fit-for-purpose technology. It is more important than ever to have your patient engagement activities unified with your data management. The shift towards technology has increased the importance of a single vendor to cover those needs. In this webinar, EvidentIQ will show you how you can have a fully unified clinical trial, including eConsent, eCOA, EDC, IWRS, CTMS, eTMF and so much more. Being able to have one vendor and one software platform to cover the entirety of your clinical trial ensures consistent ROI, consistency of support, as well as user and customer adoption. Training times are lowered, users are empowered and the data quality on the other side is so much higher.
This webinar will show participants how EvidentIQ will:
- Ensure consistent and timely study ROI and patient ROI
- Eliminate paper from all aspects ofthe trial
- Reduce the site monitoring burden wherepossible, with reduced source document validation
- Increase patient compliance and data quality with intuitive, easy-to-use, compliant data capture technology
EvidentIQ is a joining of best-of-breed applications across the areas of real-world evidence, patient engagement and clinical trial data management. Our goal is to bring the industry into a single unified platform across the entire trial lifecycle, including patient insights, clinical data management and clinical study and document management. All of this is covered within one unified, cloud-based platform.
Speakers
Andreas Weber, CEO, EvidentIQ Group GmbH
Andreas Weber is the CEO of EvidentIQ Group GmbH. With a strong background in Strategy Consulting, Andreas Weber has been supporting the life sciences industry for more than 20 years. He looks back on a career with top management positions at ERT, Bioclinica and Oracle Health Sciences.
Message Presenter
Simon Taylor, Head of Solution Consulting, EvidentIQ Group GmbH
Simon Taylor is the Head of Solution Consulting at EvidentIQ, focusing on demonstrating the unified suite to prospects and customers alike. His background is across the eClinical spectrum including clinical operations and data management. Simon started his career in regulatory affairs before bridging into the world of software.
Message PresenterWho Should Attend?
- Heads of Clinical
- Heads of R&D IT
- Heads of Real World Evidence (RWE)
- Clinical study and Data Managers
- Procurement and Category Managers
What You Will Learn
- Ensure consistent and timely study ROI and patient ROI
- Eliminate paper from all aspects of your trial
- Reduce the site monitoring burden where possible, with reduced source document validation
- Increase patient compliance and data quality with intuitive, easy-to-use, compliant data capture technology
Xtalks Partner
EvidentIQ
EvidentIQ is a next generation technology-amplified data science group championing new standards in value creation and innovation driven relevance for customers. The EvidentIQ offering brings a pioneering end to end eClinical solution that meets increasing customer demand across clinical operations and clinical data management needs with a suite of applications within a single integrated cloud platform. By combining its platform with a broad data science service portfolio such as patient recruitment, patient engagement media and a host of RWE late phase solutions EvidentIQ significantly helps customers optimize HTA submissions, pricing and reimbursement needs. EvidentIQ supports 15 of the top 20 pharma companies through novel RWE solutions and 150+ SMB customers in over 20 countries, including US, Germany, France, UK, Italy, Japan and China.
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