Viedoc vs. Mosio vs. Medable vs. EDC Made Easy

Viedoc creates innovative software that enhances the efficiency of clinical research, ensuring that essential treatments are delivered more swiftly to those in need. Our commitment lies in the realms of life and science, recognizing the strength of our collective efforts to transform the world and foster a healthier tomorrow. This unparalleled motivation drives us to continuously innovate, expedite, and refine all facets of contemporary clinical trials. Established in 2003, Viedoc has brought together scientists and clinical trial experts with a common goal of advancing transformative research. Our platform has supported thousands of studies, successfully gathering data from over a million patients while enabling seamless data transfer across various locations and countries. We take immense pride in our role in connecting patients with researchers, ultimately fostering the potential for groundbreaking advancements in medical research. Each day, we strive to bridge the gap between science and real-world impact, making a meaningful difference in people's lives.

Mosio empowers research teams to enhance participant engagement, streamline communication, and gather data effectively through the widely used medium of text messaging. Our platform offers research teams the tools to interact more effectively with participants via mobile devices, integrating engaging elements and automated messaging features. WHO CAN BENEFIT? + Sponsors of clinical trials in the pharmaceutical and biotech sectors + Cancer treatment facilities and organizations focused on clinical research + Studies funded by the National Institutes of Health (NIH) + Agencies dedicated to public health + Professionals such as clinical trial managers, directors, project managers, principal investigators, and coordinators, along with all research personnel involved in participant communication. ADVANTAGES + Engaging medication reminders and alerts for compliance + Automation of the data collection process + Boost in participant engagement and adherence rates + SMS reminders for appointments to reduce no-show rates + Improved participant retention through automated check-ins, ensuring ongoing communication and support. Overall, Mosio serves as a vital tool for enhancing the efficiency of clinical research endeavors.

Medable provides a cutting-edge software platform tailored for the research and execution of clinical trials in a decentralized manner. This innovative technology is designed to engage patients remotely, ensuring the accuracy of data collection. Moreover, patients have the ability to give their consent for digital assessments from their own locations, while the platform adapts to various local languages and regulatory standards. You can optimize your protocol’s decentralization through our flexible, modular digital and decentralized clinical trial (DCT) platform, enabling extensive remote screening across the globe to meet your enrollment targets more efficiently. Create customized screening assessments that address your specific requirements, and improve the clarity of consent documents with responsive designs that work seamlessly on both web and mobile devices. Our remote eConsent experiences provide patients with a user-friendly interface akin to popular consumer applications. With our platform’s adaptability to local laws and languages, we ensure global flexibility to cater to a wide range of needs. By actively involving patients and minimizing the challenges tied to travel and scheduling for on-site visits, we significantly enhance patient access and engagement in the research study. This method not only streamlines the clinical research process but also emphasizes the importance of patient convenience and participation, ultimately fostering a more inclusive and effective research environment. In doing so, Medable redefines the way clinical trials are conducted, paving the way for a more patient-centered approach to medical research.

Marvin is a comprehensive software platform that delivers a variety of solutions for Clinical Data Management. Its offerings encompass EDC—featuring IWRS/Drug Management and WebPRO—alongside reporting, Coding and Composer for CDISC ODM-based study design, SDTM mapping, SDTM visualization, Clinical Document Management (eTMF), and a mobile application facilitating direct communication between Investigators and patients. The technical support and software solutions provided are designed to expedite clinical trials globally. Established in 2002, XClinical stands as an international vendor in the eClinical space. By integrating advanced features, Marvin helps streamline the entire clinical data process, ensuring that researchers and healthcare professionals can collaborate efficiently and effectively.