Clinical Ink

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Clinical Ink, a global clinical technology company, offers data certainty from source to submission. Our eSource clinical technology and configurable ePRO and eCOA modules — a suite of solutions for capturing and integrating electronic data from sites, clinicians, and patients at its source — naturally enhance your clinical trial workflow by reducing manual labor, providing anytime, anywhere data access, and saving resources as your trials progress. Accelerate the completion of key clinical development milestones in your study and confidently manage your trial’s critical decisions with our flexible menu of collaborative services, remote monitoring support, and a complete, real-time view of your trial. To learn more, visit www.clinicalink.com 

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Contact details

+1 336 714 7402
info@clinicalink.com
https://www.clinicalink.com/

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Enhance Your Connected eSource Ecosystem With Lunexis ePRO+Lunexis ePRO+ enhancements provide the adaptability to support clinical trial patients and their physicians in today’s unpredictable world
Schedule a DemoImagine a trial where data streams and work flows. Schedule a demo to get on the path to cleaner data and confident decisions with Clinical Ink.
eSource EcosystemExplore Lunexis™, a clear and connected eSource Ecosystem that delivers purpose-built data capture solutions for your protocol at the moments that matter.
Bring Your Own Device (BYOD)Clinical Ink is the bring your own device (BYOD) leader. We have BYOD experience with 15,000 patients in Phase I–IV+ trials, and we offer rapid build times.
Risk-Based Monitoring StrategiesLearn key strategies to confidently develop an effective RBM strategy supported by the right tools and technologies.
Deploy Configurable, Mixed-Modality ePRO Solutions, FastCapturing, validating, and integrating patient data in real-time is an important step along the path to accelerated execution in clinical trials.
Successful BYOD in Any PhaseOur white paper discusses BYOD advantages and misconceptions, regulatory, copyright, and equivalency considerations, and a Phase III case study.
eCOA Solutions Capture and Validate Data Faster and Better, in Real TimeLearn more about how Clinical Ink’s agile Lunexis™ technology accelerates study completion.
Leading Pharma Takes Control of Infectious Disease Trial With Real-Time DataSee how a rapidly deployed Lunexis™ eSource Ecosystem (integrated eCOA, ePRO+, DDC, and eConsent) had this trial moving in 10 weeks — read the case study.
Lunexis™ Clinical Trial Empowerment ModelFind out how you can create new revenue streams, improve study oversight, and accelerate timelines with this new data collection solution.
EDC vs DDC InfographicDirect data capture (DDC) and EDC may sound the same. But a closer look reveals fundamental differences with crucial implications for clinical research
The Lunexis™ eSource Direct Data Capture (DDC) SolutionDownload this free fact sheet to learn more about how Clinical Ink’s agile Lunexis™ technology accelerates study completion.
Empowerment Model: Maximum Efficiency, Cost Savings, and ControlThe Empowerment Model is a first-of-its-kind approach that lets you subscribe to as much Lunexis as you need to build, manage, and run studies yourself.
Clinical Ink: Confident Decisions, FasterImagine a Trial Where Data Streams and Work Flows
Decentralized TrialsClinical Ink is the leader in decentralized trial conduct. No matter your goals, we have the experience to virtualize whatever trial you present us.

Team

CC
Chris Crucitti
Chief Commercial OfficerClinical Ink
DB
David Blazejewski
Sr. Director, Business DevelopmentClinical Ink
Donna Fontaine
Donna Fontaine
Global Head, Inside SalesClinical Ink
ES
Emmy Shelton
Data and Analytics ManagerClinical Ink
FD
Frank DiMartini
Director, Data ServicesClinical Ink

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