Sponsor was challenged with lengthy, resource-intensive processes to support compliance in clinical trial registration and results reporting.
A global top 10 clinical trial sponsor was challenged by lengthy, resource intensive processes to support compliance in clinical trial registration and results reporting. The Company wanted to improve these processes and reduce the time and cost of maintaining compliance.
The sponsor team was also having difficulty managing dynamic clinical trial data that was being pushed to registries and simultaneously to the sponsor’s own public website. Inconsistencies between the sponsor site and registries required double data entry and redundant quality control processes requiring additional resources, time and costs and increased the potential for errors.