Give your staff the knowledge and resources they need to conduct the trial with our full 21 CFR Part 11 compliant, certified, tracked, and localized essential protocol training, GCP training, safety, etc. Our expert team will take your protocol and bring it to life in video format so that everyone working on your study is trained consistently regardless of their location. Make sure your site staff are trained and ready to see patients for your study and give your monitoring team a ready-made clinical trial training solution so they can focus their on-site time on other activities.
Once the patients begin study visits, guide your site staff to conduct the trial compliantly using virtual patient calendars and reminders, visit-by-visit walkthroughs, and controlled document repositories. Leverage Longboat’s smartphone and tablet compatible platform to make sure your site has the knowledge and resources at their fingertips to do the right thing at the right time. Provide sites with ready-made support and guidance so that they can focus on the patient during the visit.
Update site staff and clinical research associates in real-time while they are on the move via email and SMS. With our one-click “Read and Understood” and “Electronic Signature” functionalities, you can be sure that essential study communications, documents and alerts are being received loud and clear.
Reduce the burden on sites by providing a ready-made individualized patient support platform. Better informed patients result in greater retention, reduced “lost to follow-up”, and smoother visit conduct. Also includes patient-facing videos designed to make the informed consent process easier for site staff.
Using Longboat’s Protocol Amendment Dashboard, give your principal investigators the confidence that all members of their team are utilizing the latest, IRB-approved, protocol version for their site.
Streamline the pre-screening process by quickly and easily generating electronic pre-screening logs using any device.
Make your patient feel part of the trial team with a regulatory compliant platform that enables you to provide practical support and helpful information throughout the study.
Guide your patients through each and every trial visit with email/SMS reminders, and clear patient-centric instructions on what to do before, during, and after the visit - all in their own language.
Keep the patient connected to and engaged with your study with regular updates e.g., study progress, milestones achieved, therapeutic area information, mid-point surveys, study newsletters.
Take control with real-time actionable oversight of overall and individual site performance. We give the study and monitoring teams the tools to identify and resolve engagement and compliance issues early and reinforce risk-based monitoring.
Update site staff and monitors in real-time while they are on the move via email and SMS with full audit trail for your CTMS. With our one-click “Read and Understood” and “Electronic Signature” functionalities, you can be sure that essential study communications, documents, and alerts are being received loud and clear.
Get early oversight of patient recruitment and pre-screening at study, country, and site levels, with the ability to analyze and report on pre-screening activity and identify the main reasons for non-eligibility. Quickly and accurately identify sites with an appropriate population of suitable patients, based on the study eligibility criteria.
Deploy amendments to sites as soon as they are approved locally with just a click of a button. Track confirmation of receipt and alignment to the amendment at the site level using mobile-enabled study alerts to make sure everyone is working to the correct version and avoid amendment-related findings and headaches.
Support patients throughout their trial journey with information about their progress on the study and their upcoming visits. Includes 24/7 mobile access to the latest study news and updates, the ability to opt-in for regular communications and visit reminders/guidance direct to their device via SMS or email, and communication of those crucial end-of-study results.
Study-specific training allows flexibility around on-boarding of new staff both at the beginning and during the study. Traditional Investigator Meetings and Site Initiation Visits can now be a more engaged discussion on detailed elements of the protocol and methods of recruiting than the death by PowerPoint most site staff are used to.