Early-phase clinical trials require precision and agility. Yet, managing protocol changes, patient cohorts and investigational product (IP) supply can quickly become a logistical challenge. Adaptive trials require faster decision-making and
Clinical trials are becoming increasingly complex, with a growing volume of data, forms, and regulations to manage. How can sponsors and CROs navigate this rising complexity while maintaining speed, quality,
This webinar explores the essential strategies and solutions for efficiently navigating clinical trial data collection, technology integration, and strategic planning to achieve FDA approval and secure payer reimbursement.
This webinar explores the essential strategies and solutions for efficiently navigating clinical trial data collection, technology integration, and strategic planning to achieve FDA approval and secure payer reimbursement.
Watch this on-demand webinar for expert insights from Roche Diagnostics on scaling and standardizing clinical operations with a CDMS / EDC system.
Join industry experts as they discuss the challenges digital health technology organizations face in realizing their solutions’ impact.
Join the insightful webinar on the evolution of clinical technology, growing complexity of clinical research and uncover the current challenges and gaps in eClinical tech. Our esteemed speakers, including Medrio’s CEO Nicole Latimer, will share their expertise and discuss the future of trials.
Join Freenome’s Yontao Lu, Ph.D., and Aijing Gao, along with Medrio’s Melissa Newara, as they discuss best practices and share case studies on how to achieve scale without compromising patient needs.
The Medrio and Pharmaseal partnership offers a validated data integration solution that simplifies study management. Learn how their integrated EDC and CTMS can eliminate data discrepancies and manual validation in this webinar.
In this webinar Nicole Latimer and Melissa Newara are joined by Dr. Frances Rubenstein from Nevro to discuss how Nevro, a medical device company, implemented ePRO to close gaps in data accuracy, reduce context switching for staff, and enhance patient convenience.
In this webinar, we will explore the powerful way that ePRO and eConsent tools, when implemented effectively, can enhance the participant experience and improve compliance while reducing the burden on site staff.
Many early phase studies rely on manual methods of managing participant randomization and the study supply chain. But increasing complexities in both study design and global supply chain necessitate more flexible, responsive solutions for early phase studies, in particular.
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