Access to any program features through the browser
FDA compliance: Title 21 CFR Part 11
Audit Trail, Data Query
Inspired by the researchers
Transfer your research and medical records to a digital world.
Clinical and Observational Trials
eCRF.bizTM biostatistics and data analysis centre concerns itself with data processing from various commercial and non-commercial research projects, including clinical, observational and educationel ones
Our company offers electronic research system dedicated to any type of medical research. eCRF.bizTM is modern software designed by BioStat® company.
BioStat® company with its fourteen years of experience in various research projects carried out for concerns or pharmaceutical companies offers professional and technical eCRF.bizTM support.
We provide our clients with professional support throughout the project.
Electronic case report form
FDA compliance: Title 2 CFR Part 11
Trainings for researchers
On-site research monitoring
Statistical analysis plan
Selection of sample size
Research design in collaboration with Key Opinion Leaders
Preparation of research documentation (research records, statistical analysis plan, observation questionnaire, materials for patients)
Support in research results publication
Key Opinion Leaders support in research results preparation for scientific congresses and symposia
Negotiations and contracting with medical centres and researchers
Accounting and financial settlements for centre researchers, researchers and participants
Reporting to Bioethics Commitee and URPL (Deparment of Registration of Medicinal Products)
electronic Trial Master Files
Designed by professionals
eCRF.bizTM is an integrated research platform which completely eliminates paper clinical observations questionnaires. It allows for complex research project management in terms of having access to the research background and monitoring every stage of the project by anyone involved – the sponsor, CRO and the User.
The eCRF.bizTM software was designed and produced by BioStat® Sp. z o.o.