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Brightech is recognized as an innovator shaped by our industry-leading approach, clinical data methodology and client-centric focus. Our integrated and comprehensive clinical data management approach results in a high quality seamless end-to-end management of your clinical trial data. We develop a partnership with our clients that enables effective decision-making and cost efficiencies.
At Brightech, we understand the complexity and importance to generate clinical documentation. Our team consists of medical writers and physicians experienced in clinical trial development, regulatory reports and submission documents. Throughout the clinical production phase we compile all scientific findings that may impact regulatory approval as well as product sales.
Brightech’s Clinical Information Management Suite (CIMS) is a comprehensive, fully validated, 21CFR11 compliant and fully customizable web-based clinical trial platform. This integrated proprietary system provides significant time and cost savings by sharing clinical trial information and data across all functional components during the course of the clinical trial process.
China has become a global market in many aspects. The region has great potential for the biopharmaceutical and medical device businesses. Many global organizations have established or are planning to establish clinical trial/data centers in China. With this emerging market, it is now even more essential to partner with a CRO to support your clinical development needs.
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