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ClinicalTrialsNet has developed a clinical trials software system that allows research personnel to easily conduct their activities in full compliance with HIPAA and FDA regulatory guidelines.
Project and data management for both paper-based and web-based studies are combined in one online environment to facilitate fully centralized research management. This benefits not only researchers but also those supporting researchers, such as monitors and compliance offices. All trial data and documents are entered, stored, and managed through a system that allows users to efficiently organize and conduct study activities, from study proposal and initiation, through data collection and management, to study archiving of forms, data, and metadata. The system was designed to encourage full compliance with all regulations and guidances applicable to clinical trials, including HIPAA, 21 CFR 11, and the FDA’s Guidance: Computerized Systems Used In Clinical Trials.
Our intuitive user interface makes it easier for you to focus on research, instead of research management. Specific functions include project and document management, double entry of form data, data validation rules, automatic and manual data flags, complete audit trails and trial status reporting. The only requirements are internet access and Microsoft Internet Explorer 5.5 or greater.
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ClinicalTrialsNet has developed a clinical trials software system that allows research personnel to easily conduct their activities in full compliance with HIPAA and FDA regulatory guidelines. Project...
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