Changing Clinical Protocols from Documents to Data
By leveraging data and analytics in protocol design, Faro Health CEO Dr Scott Chetham argues, sponsors can unlock automation, make data-driven decisions, and reduce patient burden.
By leveraging data and analytics in protocol design, Faro Health CEO Dr Scott Chetham argues, sponsors can unlock automation, make data-driven decisions, and reduce patient burden.
Patient recruitment and retention are some of the most significant challenges to the successful completion of a clinical trial. As
Faro Health’s Study Designer streamlines the development of clinical protocols by overcoming inefficiencies in traditional processes, enabling clinical scientists to optimize their work and better serve stakeholders and patients.
This webinar will provide a clear framework and methodology to optimize the design of clinical trials to achieve key outcomes in resource-constrained environments.
This webinar will provide a clear framework and methodology to optimize the design of clinical trials to achieve key outcomes in resource-constrained environments.
Join the featured speakers as they discuss some of the factors underpinning the lack of patient diversity in clinical trials.
By bringing words and data together into a digitized, source-of-truth SoA, study teams can effectively balance the complexity of protocol design and enable seamless digital data flow to drastically reduce study build times from months down to days.
Join our exclusive webinar, where our experts delve into groundbreaking AI implementations, revolutionizing medical writing and regulatory documentation.
Imagine how a clinical trial protocol design can be done and implemented in days. This vision is becoming a reality with the use of smart templates to build trials.