Our data management sub-division assists with the design, collection, and management of study data for a clinical research study. This group creates electronic case report forms (eCRFs) and eCRF completion guidelines for each study and will provide hands-on database access and study-specific training. In addition, our data management group oversees the development of a data management plan (DMP) for each study. The DMP is a collection of documents that outlines the methods used to manage the data within a trial. It contains the specifics on how to validate and review the data in each study. Our main goal is to produce statistically analyzable data and at the same time, ensure that the integrity of the data is maintained throughout the study. Our data management team will provide efficient, organized, and reliable resources to assist in the clinical research process.
