The complexity of the clinical trial industry is increasing dramatically year by year. We asked ourselves: what value can we bring to our customers? And our answer is: our solution has to reduce the load and save time. Driven by this idea, we developed OnlineCRF and deliver a ready-to-go EDC system, minimizing customer’s time and efforts for data collection and data management.
Co-Founder, Deputy Director
The most important drivers of our business are the ability to solve the most difficult tasks in the face of modern constraints. We apply our strengths as effectively as possible and get a great result via clear coordination of the IT, Data Management, and Clinical Operations teams.
Co-Founder, Technology Director
Passionate about developing an efficient and flexible tool for data collection in Clinical Trials, I lead the development and implementation of new features and optimization of the interface. We never stop improving OnlineCRF so that it is simple and can quickly adapt to the needs of any, even non-standard, project.
I help determine the direction of development, inspired by many years of experience in the pharmaceutical industry. I'm glad to share insight from the point of view of the sponsor and experienced EDC system user.
Head of Data Management
I enthusiastically lead the processes of preparing and setting up system testing for the client. My work is focused on OnlineCRF corresponding to all parameters of the project and being as convenient as possible for users.
Data Validation Manager
My main goal is to create an easy and efficient EDC system without inconsistencies and errors for the client's team. To do this, I meticulously develop a system validation scheme for each project's system individually. This helps to take into account all the features and checks all, even non-obvious functions and parts of the system.
Head of Clinical Operation
I believe that the guarantee of an effective and useful EDC is in full compliance with the needs and characteristics of the trial. Therefore, I oversee the audit process of project documents (Protocol, CRF). I analyze the specifics of the study and choose the best options for how all the features and requirements of the client can be implemented in an EDC system.
Associate Project Manager
I am focused on the preparatio of clear and understandable documents based on the protocol and the CRF, which will become the basis for the configuration of the EDC system. I work hard on every project parameter and the client’s requirement so that the final EDC system can meet the needs of clinical research 100%.
Wita Stwosza 16, 50-148,
Phone: +48 71 880 86 04
Our goal is building long-term relationships with clients and running excellent projects. Therefore, we offer free 30-minutes consultations on any questions related to clinical trials and clinical data management. We will be happy to provide a practical advice and clarify some elements of your clinical trials.
Please provide us with the basic information and we will get back to you within two business hours.