For national and international sponsors / CROs, we also take over the project management for multicenter clinical trials in the EU. As the project manager, we oversee the entire trial and human resources management – as well as administrative tasks – so that you receive all services from a single source.
Fewer visits to the trial center, more patients included: home care visits can benefit both patients and sponsors/CROs. Invisio recruits, places, and trains medical staff to perform study-specific tasks at the homes of study participants in compliance with GCP and protocol.
Another component of our work is trial portfolio optimization. In other words: We analyze all trial projects that have already started or are being planned in your center and identify potentials for improvement. As we are in active exchange with our partner centers throughout Germany, we have a good overview of new and existing patients and can demonstrate a very good recruitment process for our trials. In addition, we use a control system that compares each newly diagnosed patient with available trials and informs the physician about possible trial participants.
If you would like to serve as a trial site, we will of course also advise you on the selection and feasibility of trial projects. In this way, we reduce the number of trials that have to be closed again without recruitment. In order to make things as easy as possible for you, we also carry out the complete preselection of trials.
We recommend that each site define and apply a standard operating procedure (SOP) for its clinical trials. These regulations describe the standardized procedure for all work steps, whereby processes can be made legally compliant and more efficient. Does your site still work without SOPs? We will be happy to help you by creating individual SOPs for you.