OpenQ offers a powerful suite of tools for phase 4 clinical trials with a focus on delivering regulatory compliance and maximizing efficiency.

OpenQ can help you:

Collect Study Data - Create an Investigator Portal - Study initiation and review, data collection, study initiation, milestone tracking, patient enrollment information, drug shipment requests and reporting are part of the core functionality of our web-based portal. Our workflow-based engine enables easy configuration of the portal to match your business process. Study tracking and enforcement (e.g., milestone alerts) are simplified with tools for organization and custom user views that show pending tasks.

Identify Investigators - We collaborate on developing objective criteria for investigator selection and segmentation.  Then we perform an extensive search to find the right investigators for your trials.

Develop Investigator Profiles - OpenQ uses a comprehensive set of public and private data sources and proprietary technology to build detailed profiles of your selected investigators.  Screen investigators against state and federal licensing boards to uncover any past or pending actions such as debarment.