R3 Contract Management for GovCon
R3 Contract Management for GovCon offers a practical, adaptable, and cost-effective software solution tailored for small to mid-sized contractors working with the Federal Government. This platform enables organizations to efficiently oversee their contracts, subcontracts, modifications, CDRLs, CLINs, and DFAR clauses. By consolidating all contract-related information into a single system, users can swiftly access relevant data, effortlessly generate contract briefs, and effectively handle their CUI/ITAR in a system that complies with CMMC standards. Additionally, the user-friendly interface enhances productivity and streamlines the overall contract management process.
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OpenClinica
OpenClinica stands out as a prominent provider of software solutions for managing clinical data. Their robust tools are designed to enhance the compliance and efficiency of clinical trials. The main offerings from OpenClinica include OpenClinica Enterprise, OpenClinica Participate, and OpenClinica Randomize, which together facilitate a comprehensive approach to clinical data management. Each product addresses specific needs within the clinical research landscape, making them essential for successful trial execution.
OpenClinica is an industry-leading platform that enables more efficient and effective clinical trials by providing a comprehensive range of tools for managing data, patient engagement, and recruitment. Key features include electronic data capture (EDC), patient-reported outcomes (ePRO), and fully automated eConsent, all designed to improve accuracy and streamline study workflows. The platform supports EHR-to-EDC integration, reducing manual errors and accelerating data collection. OpenClinica also offers robust reporting and data analysis tools, ensuring real-time insights into trial progress. With over 15,000 studies powered and more than three million patients involved, OpenClinica is trusted by life sciences organizations worldwide, from pharmaceutical companies to academic researchers and government bodies. Its seamless integration, user-friendly design, and comprehensive features make it an essential tool for advancing clinical research.
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OnCore
Gain a thorough grasp of your research functions by implementing a comprehensive and standardized clinical trial management system that has been crafted in collaboration with leading academic medical and cancer institutions. Optimize billing designation workflows to facilitate consistency across different teams and platforms. Refine your budgeting methodologies, guarantee precise charge routing, and conduct more efficient audits and monitoring of billing compliance. This cohesive strategy offers extensive visibility and understanding of all facets of clinical research, especially in financial oversight, due to partnerships with top-tier research organizations. Additionally, by linking OnCore with your current electronic medical records (EMR), including smooth integrations with systems like Epic and Cerner, you can greatly enhance patient safety, reduce redundant data entry, improve billing compliance, and increase overall operational effectiveness. This advanced system not only streamlines processes but also cultivates a more productive research atmosphere, ultimately leading to improved outcomes in your clinical initiatives. Furthermore, the integration of these advanced technologies may lead to a more collaborative environment among research teams, fostering innovation and excellence.
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Teckro
Teckro's innovative clinical trial software effectively connects all study participants to critical information, guaranteeing accessibility at any time and from any location. In today's world of smartphone convenience, we continuously discover new solutions—so why not extend that convenience to clinical trials? Research teams and Clinical Research Associates (CRAs) can effortlessly access important and up-to-date data exactly when and where it is needed. A simple tap on a mobile device grants research personnel immediate access to essential details, creating a seamless link for those involved in the study. In addition, site staff and monitors receive real-time notifications regarding any updates or modifications that may arise. Teckro's cloud-based clinical trial software is remarkably easy to deploy, requiring no cumbersome installations, and is crafted to be intuitive and user-friendly. The platform is securely hosted and complies with vital industry standards, including FDA 21 CFR Part 11, ensuring data integrity. By guaranteeing that only the authorized and correct versions of study documents are accessible, Teckro alleviates the complexities associated with managing document versions. This forward-thinking strategy not only boosts operational efficiency but also enhances collaboration among all parties engaged in the clinical trial process. Ultimately, Teckro transforms the traditional landscape of clinical trials into a more streamlined and effective experience.
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