Learn more about the industry’s first eClinical Supply Chain Management platform
Learn why over ### major biopharma clinical trial sponsors and CROs have adopted Slope since 2020
Learn why over ##### sites across the world use Slope to manage their clinical trial inventories every day
Take the chaos out of your clinical trial operations with the Slope eClinical Supply Chain Management platform
Many dynamic, moving parts go into the execution of a clinical trial—the protocol, amendments, patient visit schedules, different procedures at different timepoints, Investigation Product (IP), lab kits, clinical supplies, biological samples, and shippers—creating logistical challenges that reduce productivity, increase costs, cause subject attrition, and threaten the overall success of the clinical trial.
There are many contributors to a successful clinical trial that keep everything moving—each with its own processes, hours of operation, systems, best practices, goals, and priorities. Keeping everyone working together effectively so that subjects have a positive experience takes a lot of coordination and communication—and it's difficult to prevent balls from dropping.
Slope provides a collaborative workspace, configured specifically for your protocol with predefined workflows and processes for supply procurement and shipping, inventory management, subject procedures, and biological sample collection and processing. Slope then uses clinical supply demand data captured at the patient level alongside real-time data and guided workflows to orchestrate the operational execution of complex study protocols. All actions taken are logged in a central source of truth for you, your investigators, and auditors.
Between all the collaborators—sponsors, sites, IP suppliers, supply vendors, labs, biorepositories, and couriers
Into trial execution and the location and status of all clinical supplies and biological samples across all collaborators
For all biological samples, investigational product, and clinical supplies whether stored or in transit between collaborators
To the protocol, amendments, and federal regulations including Title 21 CFR Part 11 GCP, ALCOAC and Sunshine Act
Take control of your clinical trial and know what is going on with your supplies, biological samples, subject procedures, and collaborators on a day-to-day basis, so there are no more surprises.
Make the most of your budget by standardizing supply purchases and operationalizing lab kit reorders, so that every biological sample collected adheres to the protocol and counts.
Get your collaborators on the same page and working consistently, correctly, and efficiently with best-practice workflows and processes that you define, control, and track.
Keep your valuable clinical trial subjects participating by making sure research sites are prepared for every visit, have the right lab kit for each procedure, and ship samples so they don’t get lost or spoil.