We bring extensive experience in project management and data collection.
Ad-hoc data collection platform
and management of the procedures for the launching of any research project.
We design the necessary material for the development of the study (protocol, CDR, patient information sheet, informed consent…) and carry out the procedures for its initiation (ethics committee, insurance…). In addition, we monitor, analyze and interpret the data generated.
Electronic data collection notebook, multi-center management, follow-up, monitoring...
Materials required
Design and elaboration of materials necessary for the realization of studies:
Protocol, CRD, informed consent, patient information sheet...
Start-up
Management of the necessary for its start-up:
Procedures with doctors, insurances, hospitals, ethics committee, randomization...
Good management and correct treatment of data, guarantees of success in clinical research.
We are committed to an optimal methodology for data analysis, so we have developed our own data collection platform (eCRF), with which we optimize its storage for its correct statistical exploitation and reduction of data collection errors.
We accompany the complete process of data collection, from the design to the necessary preprocessing for the correct analysis. In addition, we monitor, analyze and interpret the data generated.
Advantages of using our platform with CRDe
Ad-hoc for each research
100% adaptable to your needs thanks to the sophisticated permit system.
Simple and intuitive interface
Browse fast and collect data easily without compromising on quality.
User and multicenter management
Each user intervenes by ensuring the privacy of unique access to their data.
Customizable rules of operation
It increases productivity in data collection and eliminates errors.
Unique environment
Access to all study documentation and information in one place.