Fulfill your regulatory oversight obligations through real-time visibility to clinical supply, and sample compliance down to the individual patient sample. Slope ensures data integrity of all the samples traveling along the supply chain.
Demonstrate oversight of clinical trial activities
We’re making it easier for sponsors to understand the real-time status of clinical trial activities across stakeholders, uncover risk, reduce waste, ensure protocol adherence, and adapt to amendments as they arise.
Track and trace every lab kit that exists in your clinical trial
Slope’s platform provides a full traceable chain of custody for every lab kit, on every shelf, at every site, down to its expiry date, and to the individual components of that kit.
Protocol amendments should be managed systematically to avoid confusion about the protocol version or actions needed for patient visits. Slope streamlines amendment processes and provides adherence guardrails, empowering research sites to carry out their work seamlessly — even with changes.
We needed a way to manage samples that didn’t involve piecing together data from disparate sources, only to find out that there were still gaps. For all of our studies, Slope helps us mitigate risk by giving full insight into the status of samples at every stage of their lifecycle — from site collection to arriving at their destination. I would recommend Slope to any Phase I program with sample management needs!”
Sr. Director, Translational Medicine Emerging Biotech Company
With Slope, there is no longer a blindspot between the time of sample draw at the site to receiving a report from the lab. This ensures both the sponsor and the site are meeting their regulatory obligations for clinical trial oversight.