
RXNT has spent over 25 years building cloud-based healthcare software designed for ambulatory practices and medical organizations of all sizes and specialties. Our innovative, AI-powered, and data-backed software solutions help practices grow, improve clinical efficiency, and streamline business operations—whether you're a solo provider, large healthcare organization, or billing services company.
With over 60,000 medical professionals across all 50 U.S. states relying on RXNT, our fully-integrated, ONC-certified software system includes Electronic Health Records (EHR), Physician Practice Management (PPMS), Medical Billing and Revenue Cycle Management (RCM), E-Prescribing (eRx), Scheduling, Patient Portal, mobile applications, and more. Every product works seamlessly as one system or can be used standalone, giving you flexibility to choose what works best for your practice.
Our SaaS-based Full Suite software solution integrates every area of RXNT through a secure, centralized database, enabling real-time data flow across clinical and administrative functions.
Whether you're modernizing your medical practice or scaling your healthcare business, RXNT delivers all-in-one technology to help you succeed. So far, users have transmitted over 125 million prescriptions and processed more than $7 billion in insurance claims.
Built for usability and accessibility, RXNT’s cloud-based software is available 24/7 from any device and includes mobile apps for iOS and Android. Simple, transparent pricing means no hidden fees, and every plan includes free implementation & training periods, data migration, storage, software updates, and U.S.-based customer service.
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Concentrate your efforts on delivering outstanding, data-informed care using Valant, the comprehensive EHR and practice management solution specifically crafted for behavioral health practices, regardless of their size. Valant is designed to enable you to minimize the time spent on administrative duties, allowing for more focus on providing high-quality care to both individuals and groups.
Streamline your workflow by:
- Alleviating documentation burdens with a system that automatically creates clinical narratives, nearly finishing your notes for you.
- Scheduling over 80 integrated, reportable outcome measures to be sent to patients automatically via the MYIO Patient Portal prior to their appointments.
- Allowing the system to generate a coded charge when you document appointments.
- Automating the patient onboarding experience so intake packets are readily available for patients to sign within their portal.
- Receiving service requests directly through your EHR, effectively managing new patient inquiries, and obtaining a data-driven match score for prospective patients, thereby enhancing your practice's efficiency and patient satisfaction.
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Kanteron
The Kanteron Platform integrates a diverse collection of medical images, digital pathology slides, genomic data, and patient details sourced from multiple modalities, scanners, sequencers, and databases, providing a rich data toolkit for teams across hospital networks. It particularly focuses on pharmacogenomics to prevent adverse drug reactions and supports the implementation of precision medicine at the point of care by merging previously cumbersome data on drug-gene interactions, which were often limited to less accessible formats like tables in PDF files. By leveraging key pharmacogenomic resources such as PharmGKB, CGI, DGIdb, and OpenTargets, the platform allows users to tailor their queries based on specific gene families, interaction types, and drug classifications. Moreover, its flexible AI capabilities enable users to choose the dataset that best suits their unique requirements, applying it effectively to relevant medical images. This comprehensive functionality significantly improves the accuracy of medical interpretations while promoting a more individualized approach to patient treatment. Furthermore, by bridging the gap between complex data and clinical application, the Kanteron Platform empowers healthcare professionals with the tools they need to make informed decisions.
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VSClinical
VSClinical enhances the clinical evaluation of genetic variants by aligning with the guidelines set forth by the ACMG and AMP. Its organized workflow ensures compliance with the standards established by the American College of Medical Genetics (ACMG), which are crucial for identifying and classifying pathogenic variants associated with inherited diseases, cancer risk, and rare diagnoses. The integrated ACMG/AMP guidelines for variant interpretation provide a systematic approach for scoring variants and placing them into one of five classification categories. To effectively implement these guidelines, a comprehensive analysis of annotations, genomic contexts, and existing clinical data for each variant is required. VSClinical simplifies this task by delivering a tailored workflow that assesses each pertinent criterion while offering extensive bioinformatics resources, literary references, and insights from clinical databases to support the scoring and interpretation process. This forward-thinking method aims to improve the productivity of variant scientists as they manage the intricacies of variant analysis and processing. Ultimately, VSClinical emerges as a crucial resource for expediting the understanding and classification of genetic variants within clinical environments, fostering better patient outcomes through informed decision-making. Its role in facilitating efficient variant analysis cannot be overstated, as it significantly contributes to the advancement of personalized medicine.
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