Medidata Integrations

Enhance the efficiency of your clinical studies with Clinvigilant, your global provider of budget-friendly eClinical tools tailored for CROs, Pharma, Biotech, Nutraceuticals, and academic institutions throughout both clinical and post-marketing phases. Our clients consistently choose to partner with us due to our: ♦ Rapid EDC implementation (under 4 weeks). ♦ Cost-effective solutions. ♦ Integration capabilities with third-party and legacy systems. Our cloud-based platform, hosted on Microsoft Azure, adheres to HIPAA, ICH-GCP, GDPR, and 21 CFR part 11 regulations and has successfully undergone audits by the FDA, EMA, and MHRA. The Clinvigilant eClinical suite encompasses a variety of tools, including EDC, CTMS, eCRF, eTMF, eSource, IWRS, ePRO, eConsent, and eCOA. You can select the specific tools you require, and we will seamlessly integrate them into your existing software framework. Each interaction and data exchange generates detailed Audit Trails, ensuring real-time visibility of compliant data across all relevant roles. Our offerings are modular, highly customizable, and accessible via web, iPad, and mobile applications for both Android and iOS platforms. Additionally, we support the use of Patient's Own Devices (BYOD) and can interface with various devices and wearables for enhanced data collection. With Clinvigilant, you can count on a comprehensive solutions provider to streamline your clinical trial processes effectively and efficiently. Your success in clinical research begins here.

Medidata's Rave EDC (Electronic Data Capture) is recognized as the leading system for effectively handling clinical trial data from various sources like sites, patients, and laboratories, ensuring both sophistication and security. As a key component of the Medidata Clinical Cloud™, it provides an all-encompassing platform that harmonizes multiple processes, thus removing the need for data reconciliation and enabling thorough data analysis across various studies and functions. Users are able to manage their responsibilities, studies, and sites through a unified dashboard that integrates all Rave EDC and other Medidata Clinical Cloud tools. This platform significantly reduces the risks of duplicate study master data and discrepancies, such as inconsistent IDs for identical sites across different applications. Central to Medidata’s unified strategy for Clinical Data Capture and Management, Rave EDC supports the smooth collection and reconciliation of data from an array of sources, including Medidata eConsent, Medidata eCOA, MyMedidata, Rave RTSM, Rave Imaging, and Sensor Cloud; it also bolsters data review and analysis with sophisticated tools like Rave TSDV and Medidata Detect. By offering these advanced functionalities, Rave EDC not only streamlines the data management process but also empowers clinical researchers to make well-informed decisions grounded in trustworthy and comprehensive data insights. Therefore, it plays an essential role in enhancing the overall efficiency and effectiveness of clinical trials.

Many organizations depend on Datavant for the secure integration of patient data across the healthcare sector. We have positioned ourselves as the leading and most trusted provider for health data connectivity solutions. A key aspect of our mission is to protect patient privacy; our platform is fully compliant with HIPAA standards and holds SOC2 certification. You maintain complete control over how your data is accessed and used. In contrast to others in the industry, Datavant refrains from data licensing or analytics sales, allowing us to focus solely on the vital technological infrastructure necessary for data connectivity. Datavant Switchboard is uniquely positioned as the only all-inclusive solution that enables data integration while ensuring compliance with privacy regulations and maintaining user control. By leveraging our services, you gain a holistic view of patient health, resulting in more precise insights while ensuring confidentiality is upheld. With Datavant, you can access the nation's most extensive health data ecosystem, which includes over 500 real-world data partners, 2,000 hospitals, 15,000 clinics, and 120 health plans, thereby enhancing your analytical prowess and promoting improved health outcomes. This vast network not only facilitates collaboration but also drives innovation in the management of healthcare data, creating an environment ripe for transformative advancements. As healthcare evolves, our commitment to privacy and data integrity sets us apart, making us the partner of choice in this crucial field.

Research teams are increasingly pressured to deliver improved results despite constraints in resources. The advancement of a clinical trial can be greatly obstructed by challenges such as uncoordinated systems, the need for manual data entry, repetitive processes, and scattered information. Therefore, it is crucial to implement a clinical trial management system that effectively integrates and streamlines workflows while providing full transparency; Medidata presents an ideal solution for this need. Rave CTMS is distinguished as the only data-centric platform crafted for efficient and intelligent management of the entire trial process. As an integral part of the Medidata Rave Clinical CloudTM, it includes all the essential features expected from a leading CTMS, along with additional functionalities. With Rave CTMS, your study teams gain the capability to plan and execute all clinical trials in a consistent and unified manner, standardizing activity planning and management at study, country, and site levels. This system facilitates the organization of study/site team creation and activation, tracks patient enrollment and milestones, monitors site performance, and addresses challenges effectively. Furthermore, Rave CTMS fosters improved collaboration and communication among team members, ultimately contributing to more successful trial outcomes, and ensuring that every aspect of the trial is managed with precision and clarity.