About us

Company

Our company is inspired by the idea of developing an innovative tool for clinical data collection. We constantly remember that valuable data is collecting via CRF.Digital to improve the treatment of various diseases and help thousands of people.

We save the customer time

Time is the most valuable resource. And in small and medium companies, it is often limited. EDC selection and management is a task that is really important for the success of the clinical study. Requirements of the EDC system, configuration, and validation are the time-consuming tasks, and you can reduce this burden by transferring these tasks to our CRF.Digital team.

CRF.Digital : built for clinical trials by clinical experts

Our IT solutions inspired by clinicians

Since 2005, CRF.Digital development has been inspired by its founder, who is clinical trial experts.The system was originally designed to meet the needs of small CRO Company.Therefore, it takes into account many functions and subtle settings that are important for users from small and medium-sized companies.

Internal test lab for new features

Each new CRF.Digital feature is tested by direct users: CRO Pharmaxi's monitors and project managers. If it works well, it implements the new version of CRF.Digital. Real-life feedback allows for the improvement and development of the most effective features and tools.

Certificates and Declaration of conformity

Our company is inspired by the idea of developing an innovative tool for clinical data collection. We constantly remember that valuable data is collecting via eCRF to improve the treatment of various diseases and help thousands of people.

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ISO 9001:2015 Auditor

Germany

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ISO 9001:2015 Internal Audit

Germany

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Declaration of Conformity

ISPE GAMP 5

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Declaration of Conformity

21 CFR Part 11

Standard Operations Procedures of CRF.Digital

The company has established and applies a Quality Management System according to ISO 9001:2015 standard. SOP index includes the important section of the SOPs which regulates Data Management activities as well as Crf.Digital system configuration and validation. This section entitled "DM" and it was developed in strict accordance with Good Clinical Data Management Practice standard (GCDMP). Our SOPs are not set in stone, but they are periodically reviewed and improved to be compliant to the modern requirements.

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