Clinical Trial Document Management

DataRiver has developed a system for the electronic management of the essential documentation of clinical trials on drugs and medical devices. The Electronic Trial Master File (eTMF) allows you to organize and store documents, images and other digital content necessary for conducting clinical trials.

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Pharmaceutical Sector, Biomedical, Homecare

The Electronic Trial Master File (eTMF) developed by DataRiver allows the staff of Contract Research Organizations (CROs), medical directorates, medical affairs in pharmaceutical companies, business development areas and medical marketing directions in biomedical companies as wella as physicians promoting independent clinical trials, to optimize the document management of the study through:

– the electronic management of the essential documentation necessary for activating, running and closing the clinical trial
– a constant remote updating of documentation through customized access for individual users
– a real-time and remote verification of the documentation of the clinical sites

Remote Document Verification

The system allows you to verify  documentation at clinical sites both real-time and remotely.

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Clinical Trial Progress Reporting

The system delivers constant updates on the progress status of each participating site through the consultation of online documentation.

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Online Document Management

The use of the eTMF reduces the time required for managing the documentation and activating clinical sites in the course of the clinical trial.

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RELATED TOOLS

The tools

Electronic Trial Master File (eTMF)

Web and Mobile Application for managing documents, images and other digital content essential in conduction clinical trials