Imorgon
Significantly improve the speed and quality of Radiology reporting by reducing unnecessary dictation, particularly for ultrasound and DEXA. Imorgon transfers modality measurements into Powerscribe/Fluency/RadAI merge fields/tokens, eliminating manual entry errors.
Imorgon's specialized services offer the following advantages:
- All measurements are always transferred (usually DICOM SR)
- Electronic worksheets capture findings and insert them into Powerscribe/Fluency/RadAI (rather than dictating from a worksheet)
- Worksheets with priors, calculators, and clinical decision support (TI-RADS, O-RADS, etc)
- Integrate into Epic or other EHRs
- Vendor neutral
- Support to ensure everything continues working
Significant improvement in the overhead of reporting with a quick ROI.
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PayHOA
PayHOA offers software solutions designed specifically for self-managed homeowners associations (HOAs) and condominium associations (COAs). We ensure a seamless start with complimentary onboarding, unlimited support at no cost, a trial period of 30 days, and the freedom of no contractual obligations.
Our comprehensive range of services encompasses invoicing, payment processing, complete accounting, management of documents, tracking violations, handling requests, and communication options through text, email, and direct mail, along with lockbox services, customer relationship management (CRM), website creation, and additional features to meet various needs. Additionally, our platform is tailored to enhance the overall efficiency and organization of community management.
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SimpleTrials
SimpleTrials is a subscription-based, on-demand Clinical Trial Management System (CTMS) specifically designed for sponsors, Contract Research Organizations (CROs), and research facilities. It offers a comprehensive suite of tools that streamline the planning, management, and oversight of clinical study portfolios, including features for site initiation, subject monitoring, and document management via an integrated electronic Trial Master File (eTMF). Users can take advantage of real-time analytics for their studies, detailed calendars, customizable fields and trackers, on-demand reporting, planning milestones, and the management of site contracts and payments, along with electronic documentation of visits. The platform is constructed to adhere to 21 CFR Part 11 compliance standards, providing a secure and validated environment for the handling of clinical trial data. Additionally, users can customize their tracking views, seamlessly connect with various Electronic Data Capture (EDC) systems, and utilize pre-built templates for consistent document management. By fostering enhanced collaboration among all stakeholders, the system supports more effective communication throughout the entirety of the trial process, ultimately leading to improved outcomes and efficiency in clinical research.
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Oracle Clinical One
Clinical One RTSM offers a versatile range of randomization techniques suited for both simple and complex studies, eliminating the need for programming or coding, which shortens user acceptance testing times. With the ability to self-configure your study, you can create and launch it in a matter of days instead of weeks, significantly speeding up the process. You also have the capability to monitor drug inventory levels and make instantaneous changes independently of the vendor, which helps in cutting costs associated with unnecessary change requests. By facilitating rapid adjustments, you can further reduce expenses linked to change requests and avoid delays, allowing for almost immediate study launches. This platform uniquely integrates people, processes, and data, which is crucial for enhancing the effectiveness and efficiency of clinical trials. Additionally, the incorporation of virtual elements within clinical trials not only fosters greater patient involvement but also improves the overall quality of the trial data collected. To remain competitive in the fast-paced clinical research arena, it is imperative to embrace innovative digital strategies that support quicker study start-ups, synchronize data from multiple sources, and streamline workflows. Such improvements are essential for the successful delivery of contemporary clinical research projects and ultimately contribute to advancing healthcare outcomes.
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