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.

Delibr is a specialized platform designed to aid Product Managers and their teams in streamlining the feature refinement process. With real-time collaboration, Jira integration, and AI-driven document creation, Delibr enables users to efficiently manage product requirements, track questions, and capture decisions. The platform's robust features ensure a seamless workflow, helping teams save time and improve clarity in their documentation efforts. Ideal for creating PRDs, story maps, and decision logs, Delibr is a comprehensive tool for maximizing product value.