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.
Proper data collection and processing and their treatment are critical to the success of the project.
eCRF Monitoring Platform
eCDF Platform
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 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.
Complementary Services
Our products
Machine Learning for clinical data
Applicability and dissemination of your results
Demos
Other products
Shall we talk about your project?
Whatever it takes, we can adapt!
of. p1 12-13 · 31191 Esquiroz, Navarra
NNBi
We exploit research data and create and create Apps for the use of results. Custom design specialists.