ClinDatrix has formed a global consortium with eight other CROs from around the world to support pharmaceutical, biotechnology and medical device clients with their multinational clinical trials. From our headquarters in California, we support our clients, and the other members of our consortium, with our full suite of clinical research services and technology tools.
For multinational studies, we provide project management, medical safety, data management, statistics, medical writing, regulatory affairs and quality assurance services from ClinDatrix headquarters in California. We sub-contract to our affiliated CROs for clinical project management and monitoring expertise in the languages and cultures of their countries. Their in-depth understanding of local processes and regulations helps us better serve study sponsors, investigator site staffs, and study participants. Collaborating with CROs known for their exemplary services enables us to help our clients ensure the successful completion of their studies and the integrity of their study data.
Several members of our staff also are bilingual. Among languages spoken fluently at ClinDatrix are English, French, Spanish and Russian.