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Kendle offers full-services for clinical trials in France and has a team of more than 40 experienced and qualified monitors. In addition, our offices in France provide a high level of clinical resourcing services to meet the needs of our pharmaceutical customers.
Our French offices also provide comprehensive Phase II–IV clinical services such as feasibility and site selection, regulatory document collection, monitoring and site management, project management and clinical quality assurance. Additional services via other Kendle offices include protocol design, clinical data management, statistics, medical writing, information technologies, post-marketing surveillance and health economic/outcomes research services. |
