Clinical Trials Technology Consulting

Vision Point Systems offers technology consulting for clinical trials research. Our team is experienced in developing software and IT systems that are compliant with FDA's HIPAA and 21 CFR Part 11 regulations. We are also familiar with ICH guidelines and therefore can work with our clients under a variety of environments, both here in the U.S. as well as Europe and Japan. We know how to design technology components and infrastructure to ensure accuracy, data safety, and ease of analysis.

We tailor our technology implementation using a variety of platforms including Interactive Voice Response (IVR) applications, web applications, Tablet PC, PDA devices, and integrated hardware/software for identity verification and electronic signatures. We create tools that streamline the clinical trials workflow and makes data management more efficient.

Our IVR and web applications are integrated with clinical trials to provide efficiencies in the trial process:

• Randomization
• Supply Order Entry
• Patient Diaries
• Data Collection

IVR technologies assist in the following areas:

• Project Hotline - contact trial leaders in case of emergency, or to get clarification on process rules.
• Clinical data collection
• Patient data collection
• Clinical data pooling
• Use web portal to generate case report form
• Electronic case report form

Our understanding of the domain thus makes us a uniquely qualified technology partner for companies that need leading edge technology solutions to conduct clinical trials.