Welcome to the future of medical device and diagnostic research, where Milo's eClinical suite empowers researchers to establish a versatile technology foundation that meets the diverse demands of studies and regulatory requirements.
With Milo, you can kickstart your study in as little as 4 weeks. Our suite offers robust solutions for medical device clinical trials, enabling efficient data collection and exchange with minimal training. Navigate complex regulatory requirements effortlessly using a single compliant platform. Make protocol amendments with ease, adapting to the trials of today and tomorrow.
Milo provides an accessible and self-service platform, catering to both novice and experienced users. Design and construct eCRFs, manage data, and maintain control over your study workflow. Simplify participant data collection with Milo's support and services, including SLAs, study build outsourcing, TAM, training, and IRB submission support services.
Boost patient engagement and alleviate administrative burdens with Milo's ePRO module and dedicated ePRO mobile app. Streamline data collection and improve the patient experience.
Embrace real-time biometric and digital endpoint data collection with Milo's API-first approach, featuring connected wearable devices, sensors, and API interoperability.
Ready to take your medical device and diagnostic research to the next level? Contact us now to explore the potential of Milo and revolutionize your research endeavors. Don't miss out on the opportunity to simplify data management and enhance patient engagement.