11/29/2023
🟠 Are you a PI looking for some assistance in conducting protocol-specific Study Visits (on-site and off-site) for your site’s clinical trial(s)?
🟠 Has your site/Sponsor struggled to enroll volunteers per local COVID-19 restrictions and need home-based study visits from qualified Research Professionals?
🟠 Is your site’s turn-over rate for employees so high that you are unable to depend on workers and meet regulatory deadlines?
🌺 Let us help you… We have over 17 years of experience in clinical trials, from start-up to close-out, from regulatory guidances to clinical operations, and everything that makes for a successful study completion. 🌺
🐳 We can also go directly to the Subjects home to conduct each study visit per the protocol’s “Schedule of Activities” so Volunteers do not need to leave their houses at all, if they so choose. We also offer general Regulatory and Clinical Development oversight, consulting and training, including site monitoring. 🐳
🐠 Services include but are not limited to: physical exams, EKG, vitals, data entry into EDC, EDC/source document creation, specimen collections & processing, recruiting and assistance with study-related activities such as a source of support between the PI & Study Volunteers. 🐠
☀️ JUST ASK, WE WILL ACCOMMODATE ☀️