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Being a leading contract research organization (CRO) in Taiwan, Bestat is dedicated to offering clinical services with the highest quality since its establishment in 2013. Through time-efficient clinical trial management and data processing, Bestat is well-acknowledged in Taiwan and throughout the Asia Pacific regions. As experienced professionals within the industry, we provide customized services, which can be deployed on a stand-alone basis or as part of an integrated “comprehensive-service” solution, including protocol writing with trial design, regulatory compliance, monitoring, data management, biostatistics, medical writing and project management. All activities are performed in accordance with ICH-GCP to ensure compliance with all applicable regulations and protocol requirements.

Our services cover chemical entity, biologic, medical device, cell therapy, patch, vaccine, et cetera.

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  • 01

    Protocol Design and Clinical Study Report Writing

  • 02

    Sample Size Evaluation and eCRF Design

  • 03

    Data Management and Statistical Analysis

  • 04

    Monitoring and Site Management

  • 05

    FDA/TFDA/IRB Submission and Project Management