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 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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Unlearn
Advancing artificial intelligence to eliminate the necessity for trial and error in healthcare, our digital twins enable rapid and reliable clinical trials. We prioritize research in fields such as neuroscience, immunology, and metabolic disorders, among others. TwinRCTs accelerate full enrollment by requiring fewer participants to achieve the same statistical power as traditional trial methods. This innovative strategy drastically cuts down on the time needed for late-stage study enrollment. Furthermore, TwinRCTs improve the detection of treatment effects in early-stage research by increasing statistical power without needing more participants. They allow researchers to make well-informed decisions based on initial findings and assist in attracting additional participants to clinical trials. By utilizing smaller control groups, TwinRCTs also enhance the likelihood of participants receiving the experimental treatment. Our dedication to ensuring that clinical trials with digital twins achieve regulatory approval remains steadfast. Unlearn is leading the charge in revolutionizing the healthcare industry through the pioneering use of artificial intelligence, crafting and applying cutting-edge generative models that utilize extensive datasets gathered from prior patient studies. This shift in methodology not only optimizes research efficiency but also significantly improves the effectiveness of clinical trials. The future of medicine is being reshaped as we continue to refine these innovative approaches.
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