TrackWise can be used as drug safety software by pharmaceutical/biopharmaceutical companies of all sizes to reduce product safety risk, achieve compliance and improve efficiency of pharmacovigilance processes.
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TrackWise offers a web-based drug safety system that enables organizations to accurately and efficiently record events, MedDRA code terms against industry standard thesauruses, conduct relatedness and listedness/expectedness assessments, and report adverse events to appropriate health authorities. In addition, TrackWise is fully compliant with international regulations and guidelines supporting case management, report preparation and electronic submissions. TrackWise electronic reporting capabilities include flexible mapping and configuration to meet the complex and varying requirements of global regulatory authorities.
TrackWise has a proven track record, with more than 100 pharmaceutical and biotechnology customers and hundreds of thousands of end users around the globe.