By putting the patient at the center of your next clinical trial, you can reduce staff burden, capture more timely and accurate data, and engage your study participants in ways not possible with paper or older Clinical Trials Management Systems (CTMS) / Electronic Data Capture (EDC) platforms.
A more engaging clinical trial experience with a more engaging clinical trials management system
By putting the participant at the center of your clinical study, a whole world of new possibilities emerge for understanding your treatment, medication, or device. For example, deliver tailored, trial specific content directly to study participants at the right time, automatically, and ensure that they understand your product and are adhering to your treatment protocol.
Increased data accuracy and staff efficiency with next generation electronic data capture
Collecting data directly from patients, in the moment, means no more retrospectives, giving you data that more accurately represents what is happening in the real world. It also means that staff time is not required to transpose data from paper, or other data sources, like an EHR, reducing the opportunity for errors in transcription.
Faster speed to data lock than with other clinical trials software
The faster you can achieve data lock, the faster you can move to the next phase in the development of your blockbuster new treatment. We help you get to data lock faster by giving you participants and clinical research team the tools they need to ensure they get the best, cleanest data, as early in the process as possible. Our iterative, and adaptive, approach to forms and longitudinal workflow automation, also means you can respond to what you are learning in your clinical trial, and quickly adjust to intervene when needed.
Keeping an eye on it all – CTMS / EDC in the cloud
DatStat clinical trials software solutions are based on our proven, 21 CFR Part 11 ready, and HIPAA compliant, cloud platform, and are available from anywhere in the world. Simply log in using a web browser, and you have full access to the management and status of your clinical study no matter where you are. By engaging study participants in your trial directly, you can monitor their related activities on a real-time basis, giving you more insight faster into the data that is most important to your clinical trial.
Clinical Trials Management System (CTMS)
Assemble a robust profile and history of your clinical trial, its participants, and their involvement in data collection and other clinical trial related activities. Use that profile, and data, to communicate, administer, monitor, and manage their study activities in real-time.
Provide your study participants with an easy to understand and complete, online eConsent process. You can even monitor eConsent activities remotely, alongside your other clinical trial activities, and take automated action based on them completing the process.
ePRO / eCOA
Modern clinical trials are using technology to put the patient front and center, and we provide you with rich options to directly engage them in providing data to your trial. By involving them directly in your study, you will increase participant engagement and improve retention.
Clinical Trial Automation
Easily collect and track participant data over time, with the ability to easily view and monitor participant data capture activities, all in real time. Daily diaries and check-ins with your study participants have never been easier.
Notifications & Triggers
Integrate notifications and triggers into your clinical trial study design automation and ensure your study participants are adhering to your medication, device, intervention, or protocol. Prompting your trial participants keeps them engaged across the length of your trial phase.
Electronic Data Capture (EDC)
Use one platform for all your electronic data capture scenarios (eCRF / ePRO / eCOA), simplifying your operations, data management, and user training, and with an open REST-based API, the integration possibilities are endless.
Secure messaging between participants and research coordinators has never been easier or more convenient, and with DatStat, you can rest assured that your communications are HIPAA secure and retained for future data mining of interactions.
”DatStat’s scalable and flexible technology allows us to use the power of patients to speed recruitment and development of new therapies for COPD. We are especially pleased with the engaging user experience on both desktop and mobile.”
DatStat has two decades of experience delighting customers and delivering clinical trial and clinical care solutions. Our team will work closely with your team to help you understand how our solutions can transform your next clinical trial or clinical care program. Through our proven implementation model, we will work to bring your solution to life, integrating your branding, content, and protocols, and because of our platform approach, we can take you from idea to reality faster than you ever thought possible. It really is that easy.
Let us help you transform your clinical trial and data collection activities by connecting with us today.