VSClinical Reviews

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.

An API driven by Google's AI capabilities enables precise transformation of spoken language into written text. This technology enhances your content with accurate captions, improves the user experience through voice-activated features, and provides valuable analysis of customer interactions that can lead to better service. Utilizing cutting-edge algorithms from Google's deep learning neural networks, this automatic speech recognition (ASR) system stands out as one of the most sophisticated available. The Speech-to-Text service supports a variety of applications, allowing for the creation, management, and customization of tailored resources. You have the flexibility to implement speech recognition solutions wherever needed, whether in the cloud via the API or on-premises with Speech-to-Text O-Prem. Additionally, it offers the ability to customize the recognition process to accommodate industry-specific jargon or uncommon vocabulary. The system also automates the conversion of spoken figures into addresses, years, and currencies. With an intuitive user interface, experimenting with your speech audio becomes a seamless process, opening up new possibilities for innovation and efficiency. This robust tool invites users to explore its capabilities and integrate them into their projects with ease.

Emedgene enhances the processes associated with tertiary analysis in the fields of rare disease genomics and various germline research projects. The platform is designed to improve the speed and consistency of interpreting, prioritizing, curating, and producing research reports on user-defined variants. By utilizing explainable AI (XAI) and automation, Emedgene significantly increases efficiency across a range of analysis workflows, including genomes, exomes, virtual panels, and targeted panels. It also aids in merging laboratory operations and next-generation sequencing (NGS) instruments with IT systems, thereby optimizing and securing the entire workflow. As science and technology continue to evolve alongside growing demands, Emedgene provides users with the latest advancements through innovative knowledge graph features, curation tools, and expert assistance throughout their research endeavors. Additionally, laboratories can enhance their throughput without needing to hire extra personnel, thanks to the capabilities of XAI and automated systems. Ultimately, Emedgene supports the implementation of high-throughput workflows for whole genome sequencing (WGS), whole exome sequencing (WES), virtual panels, or targeted panels, all of which seamlessly integrate into the digital infrastructure of any laboratory. This holistic approach ensures that researchers can dedicate their efforts to uncovering new insights while benefiting from reliable technological support that evolves with their needs. By streamlining these complex processes, Emedgene empowers researchers to maximize their potential and drive impactful discoveries in genomics.