Our technical activities cover the entire pharmaceutical development life cycle: from drug discovery, to clinical trial, to New Drug Application (NDA) submissions. DoubleBridge delivers solutions that help our pharmaceutical clients prioritize, plan, and implement the appropriate technological solutions to meet their needs.
DoubleBridge's solutions , knowledge and expertise cover the spectrum of innovative projects in the life science industry, including bio-informatics data management systems, laboratory data management systems, laboratory logistical information tracking and management systems, drug discovery data integration and data warehouse systems, clinical trial data management systems, validation systems, FDA/21CFR Part 11 Compliance solutions, web based auditing tracking systems, regulatory affairs document retrieval and archive systems, NDA e-Submission systems, patient monitoring systems, and pharmaceutical sales information management systems.