Clinical DataFax Systems Inc.
The DataFax clinical trial management system supports data collection by both Fax and EDC (electronic data capture over the internet) in the same study with complete integration designed to make it easy to select the method that works best for different users or data forms, and to switch methods if necessary at any time during a trial.
Since its introduction in 1991, DataFax has been used in clinical trials conducted by pharmaceutical companies, contract research organizations, universities, and NGOs; in the United States, Canada, South America, Europe, Africa, and Asia.
Our strengths include:
- Commitment - founded by clinical trialists for clinical trialists.
- Versatility - use Fax, EDC or both in the same study.
- Flexibility - switch between EDC and Fax as needed at any time.
- Scalability - used in trials with over 1,000 sites and over 10,000 patients.
- Freedom - the tools you need to setup and manage your own studies.
- Track Record - 19 years, hundreds of completed trials, scores of successful NDA submissions, and zero FDA citations.
- User Community - creative individuals working in a wide variety of clinical areas, annual User Group meetings, and a vendor audit committee.
- Regulatory Compliance - dedicated to meeting all FDA and ICH requirements, DataFax includes electronic signatures, password aging, SSL encryption, and full audit trails and reports.