Clinical trials are more complex than ever before with more endpoints, eligibility criteria, procedures and data point.
Busy site staff need clear guidance and support to navigate this growing list of requirements to all aspects of trial are preformed in compliance with GCP and the protocol to provide complete and high-quality study data. Longboat’s Visit Essentials provides site staff with precise, patient-specific instructions for each visit at the time they need it. This results in greater compliance, better data quality, and fewer protocol deviations.
“It is not enough to do your best; you must know what to do, and then do your best.”
W. Edwards Deming
In a Phase IIIb breast cancer trial including 16 countries globally, sites utilizing Longboat had 21% fewer protocol deviations than non-Longboat sites
Clinical trials have more endpoints, eligibility criteria, procedures and data points than ever before. Longboat consolidates disparate protocol information into just-in-time visit instruction so sites can focus on caring for their patients.
All relevant personnel receive reminders ahead of upcoming visits and have real-time access to same concise instructions for visit conduct, ensuring smoother visit workflow through the clinic for patients.