Take advantage of ePRO solutions and save time while increasing patient compliance and improving data quality.
Clinical trials need as much relevant data as possible about the treatment, experience of the treatment providers and direct feedback of the patients. This helps to ensure the safety and performance of pharmaceutical and medical products and to gain new insights. Patient-related data in particular is becoming increasingly important. Therefore, many manufacturers nowadays try to get feedback directly from patients. However, they often find it difficult to reach, engage and receive regular feedback from their patients. This is where ePRO comes in. With the so-called "Electronic Patient-Reported Outcomes", patients themselves provide feedback on their personal wellbeing. Using digital questionnaires or diaries, the feedback can be collected on any mobile device. Learn more about the advantages of ePRO in our video:
▸ Time savings
▸ Patient compliance
▸ Increased data quality
➤ What does Climedo do?
Climedo offers a software platform for hybrid clinical trials and observational studies. Its easy-to-use, modular and secure solutions for data management include electronic data capture (EDC), ePRO, eCOA, and Telemedicine. This enables pharma and medtech companies to validate their medical innovations more efficiently in the post-market phase and to capture data in decentralized, real-world settings. As a result, they accelerate studies, save costs, and improve data flow and quality, while fostering innovative trial designs. By connecting all stakeholders (industry partners, study sites, physicians and patients) in one cloud-based system, Climedo is revolutionizing clinical research and making trials more accessible and patient centric.
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