eCRF

DataRiver develops Electronic Data Capture (EDC) systems for the management of eCRFs accessible through PCs and Tablets. The development of these systems is compliant with the standards, regulations and international guidelines for clinical data management.

The systems allow:

  • the management of phase I – IV drug studies, observational studies and medical device studies
  • the visualization of data and statistics interesting the clinical study and the patient enrollment trend in the sites involved in the experimentation
  • the integration of data collected through CRF data sheets with data collected directly from the patient through the management of patient questionnaires and from wearable and medical devices

WHO IS IT FOR?

Pharmaceutical Sector, Biomedical sector, Indipendent Clinical Research

The eCRF systems are designed for the management of clinical trials on drugs and medical devices promoted by Pharmaceutical Companies, Biomedical Companies, Hospital,Universities and Research Foundations.

e-CRF Design and Development

DataRiver provides consultancy and support for the design and development of eCRF. The company has gained experience in the management of clinical trials in various therapeutic areas, in particular Oncology, Cardiology, Cardiac Surgery, Hematology, Infectiology, Neurology, Pneumology, Gastroenterology and Rare Diseases.

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Data Cleaning, Query, Edit and Validation Check

DataRiver manages data cleaning activities planned in the clinical protocol and query management

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Data Management Plan (DMP)

DataRiver provides consultancy and support for writing and reviewing the Data Management Plan (DMP) for phase I-IV, observational and medical device studies.

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RELATED TOOLS

The tools

OpenClinica

Electronic Data Capture System for eCRF management accessible via PC and Tablet