eHealth App xChange

Bioclinica eHealth App xChange is an alliance program for disruptive technology innovation in clinical research. It is an ecosystem of interoperable solutions that extends Bioclinica’s platform of solutions and facilitates a flexible, customized, end-to-end approach. By making a variety of eClinical technologies available and interoperable, the App xChange enhances the quality and efficiency of clinical research. Bioclinica and App xChange partners support core functions required in all clinical trials, including data capture, randomization, trial management, trial supply management, risk-based monitoring, safety reporting, eTMF, and regulatory compliance.

App xChange partners provide patient-direct approaches using apps, sensors, and wearables. These patient-centric solutions provide electronic informed consent, diaries, patient reported outcomes, patient engagement, reminders and alerts, medication adherence, caregiver communication, screening for eligibility, and symptom assessment and testing.

Become an App xChange Partner

App xChange Partners

A solution for integration all eClinical study data.

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Advanced medication adherence solutions powered by artificial intelligence, integrated with Bioclinica Express EDC.

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A modern clinical safety and pharmacovigilance platform to improve compliance with global regulatory guidelines.

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Clireo eTMF from arivis and Bioclinica's OnPoint CTMS are integrated, allowing single source data entry to populate both systems, eliminate redundant entry tasks and improve data quality.

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DupCheck is a web-based tool used globally to screen for duplicate patients and previous participation in clinical trials across studies, sponsors and therapeutic areas. DupCheck can be linked to Express EDC and Trident RTSM, eliminating duplicate data entry.

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Web-based phase 1 eSource/EDC system supporting traditional browsers and mobile devices, including extensive integration with both telemetry and cardiograph ECG systems.

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Mobile and online health platform that empowers individuals to take control of their health, from building a health profile to sharing health information, thereby securing better quality research data and running faster, more efficient and accurate clinical trials.

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Custom, cost-effective, engagement and data collection programs for research with two-way text messaging, including programs for study recruitment, patient retention, surveys, ePRO, medication adherence, compliance confirmation, incentives and motivation, and text-based interventions.

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Electronic patient-reported outcomes and clinical assessments for pre- and post-marketing research, smart patient retention and compliance solutions via SMS and mobile app, patient engagement with a smartphone app, and patient recruitment.

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Clinical 6 is a mClinical platform for patient enrollment, engagement and management.

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Enables remote monitoring of clinical trials with Virtual On Site Monitoring (VOS), which integrates high-cost traditional monitoring with an innovative method that leads to significant reduction in time and cost by eliminating the need for monitor relocation.

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Provides customized online solutions via one online platform that make investigator training for clinical trials faster, simpler and less expensive, and more compliant through robust reporting and compliance features which can integrate with Bioclinica's payment solutions.

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Adaptest® is computerized adaptive testing and item response theory (IRT)-based scoring that allows statistical information obtained during scale development to better inform the assessment process.

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TransformPVTM enables existing safety applications to transmit and receive E2B (R3) ICSR XML’s and R3 ACK files. The E2B (R3) adapter allows organizations to transform E2B (R2) files into E2B (R3) files and vice-versa.

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Global mHealth Machine to Machine (M2M) platform solutions.

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Volv Partners' mission is to speed science, reduce cost of healthcare, revolutionise finance thereby enhancing the economic output and well-being for all. We focus on complex industry challenges and how to solve them, and then apply appropriate leading edge technologies. 

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eTMF maintains trial documents in one secure, easy-to-use and globally accessible location.

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