
Beats Medical partners with leading pharmaceutical companies to enhance their real-world data and evidence collection throughout the drug development lifecycle, from pre-clinical stages to commercialization. Their cross-disease, multi-symptom platform technology, Colbolt©, offers objective digital assessments without requiring additional hardware, functioning across iOS and Android devices. The platform integrates into clinical pipelines, delivering objective assessments to improve R&D activities and offering tailored digital therapies for long-term behavioral change. Beats Medical focuses on simplifying digital strategy for clinical research by providing AI-supported digital assessments that accelerate progress and enable real-time decisions. Their solution supports various trial phases, including observational studies and clinical trials, aiming to identify the right endpoints from the start. The company has a proven track record, with a Class 1 Medical Device certified for ISO 13485 compliance, and boasts significant user engagement with 97 million steps taken by users globally across 30+ countries, leveraging 11 years of experience in digital clinical research.

Beats Medical partners with leading pharmaceutical companies to enhance their real-world data and evidence collection throughout the drug development lifecycle, from pre-clinical stages to commercialization. Their cross-disease, multi-symptom platform technology, Colbolt©, offers objective digital assessments without requiring additional hardware, functioning across iOS and Android devices. The platform integrates into clinical pipelines, delivering objective assessments to improve R&D activities and offering tailored digital therapies for long-term behavioral change. Beats Medical focuses on simplifying digital strategy for clinical research by providing AI-supported digital assessments that accelerate progress and enable real-time decisions. Their solution supports various trial phases, including observational studies and clinical trials, aiming to identify the right endpoints from the start. The company has a proven track record, with a Class 1 Medical Device certified for ISO 13485 compliance, and boasts significant user engagement with 97 million steps taken by users globally across 30+ countries, leveraging 11 years of experience in digital clinical research.