Founded forty years ago, DRS continues to build on our industry reputation for excellence in support of worldwide clinical trials.
-
DRS offers a robust electronic trial master file (eTMF) that can be implemented in a condensed timeline along with multiple custom file structures.
The eTMF platform also contains an archiving module for long term storage to meet various regulatory requirements.
-
We proactively work to ensure success in trial management by adhering to good document practice (GDP) guidelines, providing ongoing error reporting,
and facilitating timely mitigation of document issues.
-
Sponsors and CROs no longer need to shoulder the responsibility for oversight of the daily document submissions.
Proper handling of the study documents by DRS means fewer errors in your study library and higher grades for overall regulatory compliance.