NT NOVOTECH THE ASIA PACIFIC CRO

Class [042]
Computer & Software Services & Scientific Services

Conducting clinical trials for others; conducting and managing clinical trials in the nature of conducting clinical trials for others in the field of pharmaceuticals, biotechnology and other related industries; conducting clinical trials for others [scientific research]; providing medical and scientific research information about the results of clinical trials, including clinical trials for pharmaceuticals and biotechnology; scientific research; scientific research for medical purposes in the field of pharmaceuticals, biotechnology, and related industries; preparation of statistics, namely, scientific analysis in the field of clinical trial results for scientific research; preparation of biostatistics, namely, scientific analysis in the field of clinical trial results for scientific research in the fields of pharmaceuticals, biotechnology and other related industries; provision of medical and scientific research information and data relating to medical and scientific research for pharmaceuticals, biotechnology and other related industries; database design and development services to process data collected from clinical trials; medical research services, namely, medical monitoring services for research in the fields of pharmaceuticals, biotechnology and other related industries; quality audits, namely, inspection for quality control purposes and quality control for others, technology supervision and technical verification of clinical trial designs and clinical trial data; preparation of reports and applications to regulators relating to aspects of clinical trials, namely, providing medical research and scientific information and data in the field of clinical trials; provision and exchange of information and data exchange between scientists, manufacturers and health authorities relating to pharmaceutical and biotechnology quality standards, namely, providing a website featuring technology enabling authorized users to generate, manage, and exchange medical and scientific information, data and documents; technical writing of clinical report forms which are required by clinical trial drug protocols