RPI’s eTMF solutions facilitate clients’ management of data and documents for clinical trials. RPI administers the eTMF, which includes setup, processing, maintenance, and quality control of clinical trial documents for archiving and transfer to the sponsor. Our quality control process checks for document completion, accuracy, relevant signatures, and duplications. RPI’s eTMF team ensures the eTMF for each study is current and provides status reports to track outstanding or expiring documents. Upon completion of a study, the eTMF team performs a final quality check prior to archiving and creates an audit report.