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Since the establishment of the company in 2003, the Department of Statistical has become a team with more than 30 staffs after more than 10 years of continuous development. Under the guide of Dr. Meng, this team has become a strong team which not afraid of any hardship and undertake obligation.
Participating in the implementation of hundreds of clinical trial projects in pharmaceutical enterprises at home and abroad, we have accumulated rich programming experience. And the quality of our work is guaranteed through rigorous systematic training and perfect SOP. The team is also responsible for the company's innovation and R&D work, and has successfully applied for 17 patents.
Under the guidance of various clinical programmer and statistical consultants with more than 20 years of work experience in the United States, we have met the requirements of FDA. We have also introduced a set of high-standard output macro to ensure the high quality of the TFL output format. We irregularly scheduled carry out standardized training for CDISC related, such as SDTM, ADaM, etc., to ensure that our program fully meets the requirements of CFDA and FDA