Amarex Clinical Research has extensive experience successfully performing clinical studies from across all phases of research and discovery, development, validation and approval. We incorporate scientific excellence and product development strategy in all that we do. Our leadership team has the experience to efficiently provide solutions to the most demanding drug development challenges with a driven focus on completing projects on time, on budget and with the quality that will withstand the most vigorous scrutiny. Our leadership team has been involved in over 400 clinical research projects in over 35 countries. Currently we are conducting studies in the United States, Canadian, our E.U. sites and through our partners in Asia. We have conducted GCP/GMP compliance audits in the EU, Israel, China, Taiwan, Korea, South America and the United States. The leadership team has over 70 years of combined experience and expertise in conducting biomedical research, standardization of data management protocols, oversight of clinical trial operations and trial management of Phase I – IV studies of drugs, devices, botanicals, diagnostics and biologics. Their knowledge, expertise and experience in conducting comprehensive services in Project Management (Phase I-IV, BE/BA, PK/PD), Regulatory Affairs, FDA Applications Submissions, Compliance Audits, Clinical Operations, Adaptive Study Designs, Biometrics, Statistical Analysis, Data Management and General Consulting has enabled Amarex to take our clients through the entire process from the initial product concept to FDA approval and then ultimately to the market safely and quickly. We recognize and understand the importance of providing leading solutions in drug and device development and we have a strong track record in advising clients through the development process. We believe in having a data-driven approach and a collaborative partnership with our clients; working closely to ensure that we provide customized solutions for your unique clinical study.
Web: https://www.amarexus.com
Add：90000 Rockville Pike Bethesda, MD 20892 301-496-4000
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微信号：csco2022
公众号：康安医药咨询
