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TARA has been designed from the outset by pharmacovigilance professionals, supported by a team of software developers drawn from both academia and the Information Technology Industry.
This solution is a new concept in clinical safety management for both clinical trials and marketed products. The design of TARA is one of its most favoured assets; the layout is consistently simple, intuitive and most importantly user friendly.
TARA’s features have allowed dramatic improvements to the quality and speed of case processing. Enabling companies to monitor products and provide early identifications of risks and safety trends without the hassle of a dated and slow system.
TARA has been designed to be affordable for smaller and medium sized companies, as well as having the capability to deal with large amounts of data for the larger corporate companies. There is increasing need to balance regulatory and legal compliance with cost control.
