Data management consists of three parts: collection, integration, and validation of clinical data to ensure data accuracy and integrity. It is important that all project team members adhere to the data management plan and regulatory requirements. Therefore, all project team members must be trained and qualified to perform data management.
At EPS we pride ourselves in being one of the largest companies in Japan able to perform the full range of data management services for our clients to successfully register their medications on the market. In addition to Japan, we have expanded our data management capacity to Asia and SEA(Southeast Asia) to ensure we can respond to future research needs including post-marketing surveillance studies. With our current capacity, EPS can perform data management with up to 180 simultaneous protocols. We also have the capacity to integrate our data management functions to enable clients to properly comply with the Clinical Data Interchange Standards Consortium (CDISC).
A full range of data management services that are your assurance of successful clinical trials.