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This global Clinical Research Organization (CRO) offers a full range of research services to support worldwide clinical trial strategies for the pharmaceutical, biotechnology and medical device industries.
With approximately 5,000 employees across six continents and experience in more than 100 countries, the CRO’s safety specialists are responsible for the collection, translation and reporting of large amounts of technical medical data for pharmacovigilance requirements and study reporting purposes.
On any given day, the CRO’s safety specialists receive information from 350 clinical and post marketing studies taking place worldwide. The volume of incoming data is very high, with as many as 60 safety specialists at a time submitting reporting data that requires translation.