Streamline Verify is an industry-leading exclusion screening solution designed for healthcare compliance. It automates the process of identifying excluded individuals and entities, simplifying compliance with state and federal regulations such as the OIG LEIE. The platform provides features like 24-hour instant access to reports, monthly automatic re-screenings, and real-time compliance status updates. By leveraging this tool, organizations can minimize risk, ensure regulatory adherence, and streamline their compliance efforts effectively.

Genius PT is an innovative tool tailored for physical therapists and healthcare professionals. This Chrome extension automates the documentation process, allowing users to easily input and manage clinical notes, track treatment progress, and maintain compliance with medical regulations. With features like customizable templates and fast data entry, it makes patient documentation more efficient, ultimately improving patient care and saving valuable time.

eHealthGPT utilizes advanced AI technology to revolutionize communication in healthcare. By automating routine email tasks, such as appointment scheduling and prescription requests, it minimizes administrative burdens on healthcare providers. This allows for more timely and efficient patient interactions. The tool is tailored to the unique challenges of the healthcare environment, ensuring that communication is not only efficient but also secure, fulfilling regulatory requirements.

Formly provides a comprehensive solution for startups to achieve medical device certification compliance in the EU and US markets. By leveraging AI technology and a team of experienced regulatory experts, the platform simplifies the documentation process required for ISO 13485 compliance, technical documentation, and change management. Formly ensures that companies can scale according to their needs and stay updated with compliance alerts, automating tedious documentation tasks. Suitable for various device classes, it accelerates the go-to-market process, ensuring that all regulatory standards including MDR 2017/745 and US FDA 21 CFR are met.