Sponsors of global trials face many challenges. One of the most sensitive concerns is appropriate collection and handling of clinical data. Data managers face variation in data collection methods and clinical trial practices among the countries or regions participating in a global trial. PROMETRIKA’s successful approach to data integrity includes strong global oversight and advanced technology and processes.
PROMETRIKA has formed strategic partnerships with like-minded and similarly sized local CROs in over 80 countries on 5 continents. These relationships have established guidelines for working together in the sponsor’s best interest. Our international colleagues’ deep local expertise, along with constant communication and a global strategy, ensure that data quality is consistent across locations.
Global data collection strategies often include wearable devices and telehealth to ensure patient compliance. These advanced decentralized technologies lend themselves to central monitoring, which leads to more efficient data surveillance and reduced onsite monitoring costs. Near-real-time meta data can effectively identify high-risk clinical sites, efficacy and safety data trends, and data quality issues that may compromise study results. Sponsors and CROs are able to quickly address problems, saving extended costs and timelines due to unusable data.
At PROMETRIKA, we use the top-of-the-line EDC, CTMS, eTMF, eCOA, IWRS, data analytics, smart technologies, and project management platforms to provide accurate, clear metrics to sponsors. We regularly assess and quickly adopt next-generation technologies and provide a customized technology strategy based on each sponsor’s needs. We have extensive experience with decentralized clinical trial solutions that are regularly employed at the global scale. Our experts are available to propose the optimal decentralized clinical trial (DCT) model for your protocol driven needs.
