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.

Review Wizard is a powerful tool designed to simplify the process of creating comprehensive review reports. With its user-friendly interface, you can effortlessly generate detailed reviews that include key metrics and insights. This tool is ideal for businesses and individuals looking to streamline their review documentation process, ensuring accuracy and consistency in every report. By using Review Wizard, you can focus more on analysis and decision-making, rather than spending countless hours compiling data.