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Create, in a few hours, an eCRF that is as easy to use as a paper one, and avoid the biggest headaches in data collection in Pre-authorisation and Post-authorisation studies of your medical device. Incorporate an EDC that is highly flexible when creating the eCRF, this will allow you to meet the needs of any kind of study. Save tons of time in the management and monitoring of the study with the management and monitoring tools included in the EDC. Use a validated system with all the security guarantees that give trust to the sponsor and allow the collection of quality data. Don’t wait until the analysis phase to discover mistakes in the data or you will end up chasing down investigators to correct them. Prevent the process of creation of an eCRF from being long and complex.

With Tractivity's stakeholder management platform comes clarity from one system. Read more to find out how our cloud-based platform can help your stakeholder engagement and consultation projects. If improved stakeholder consultations and outcomes matter to your organisation, then we're here to help you engage, manage and deliver compelling insights and improved outcomes across your entire stakeholder landscape. When you engage with Tractivity you get access to the most up to date, relevant and practical tools to deliver impactful communications all from one system. Run successful engagement projects from start to finish with all the tools in one system. Our cloud-based platform helps you continually monitor your entire stakeholder landscape bringing the clarity you need. Our platform is designed to help you engage and capture every interaction. Tractivity gives you the tools to be creative, engaging, and to communicate your success.