CFS Clinical initiates, distributes, collects and manages all of the necessary documentation for trial activation using a suite of innovative software that largely automates the process and significantly alleviates the burden on your legal team. We also negotiate and customize informed consent between sites, investigators and sponsors.
Our contract management process is precise, efficient and transparent from our first pass in drafting trial documents through contract execution. By involving your legal department only when necessary, the negotiation and review process becomes much more streamlined and is completed with fewer headaches, allowing your legal support team to focus its efforts on making recommendations that reduce risk for your organization rather than chasing down busy investigator site staff.
Our robust global legal network—with on-the-ground resources available in 61 countries—supports contract negotiations around the world, so you can be confident that your documentation will conform to the intricacies of regulations that are outside your scope of expertise.