All you need is "CRO x IT" - Your Integral Partner for Life Sciences.

Services & Solutions

We are a group of specialists who has been involved in drug development and the marketing as a CRO. We flexibly cover wide-ranging outsourcing demands, and provide consulting services by making full use of the experience and expertise. We are also well experienced in IT system implementation because our parent company was one of the first IT companies in Japan. Our support covers all medical and pharmaceutical operations from various perspectives..

Drug Discovery & Non-clinical

We support concerns and issues in preclinical studies in flexible and wide-ranging ways.

We offer services to realize the acceleration of research operations involving drug discovery/non-clinical trials, accurate decision making, and cost reduction in order to achieve swift approaches toward the global market.

Clinical Development

We provide high-quality services as a CRO with numerous instances of success and depth of experience.

As your best partner in clinical development, ranging from medical writing, monitoring and EDC to DM, we support cost-savings and efficiency while providing value-added service.

Regulatory Operations

We offer practical outsourcing services and tools for global regulatory application.

We provide contract services for CTD/eCTD compilation and New Drug Application (NDA)/Marketing Authorization Application (MAA) support services that meet optimal balance among nature of application, volume of data, and total cost. Moreover, we present a line of tools with functions specialized in NDA/MAA. These tools are also independently available.

Life Cycle Management

We strongly promote Early Post-marketing Phase Vigilance and Post Marketing Surveillance and support customers with lifecycle management.

In order to effectively collect quality information and streamline and speed up business operations, we offer a system with services of user-centered designs for MR and management department.


We provide a full range of services to promptly and adequately collect, evaluate, report, and utilize adverse events.

In order to realize quick, quality pharmacovigilance operations suitable for the risk management required by pharmaceutical companies, our total support system covers from system structure planning, implementation, development and to operation assistance.


We conduct a consultation with an emphasis on the essence of your needs and propose an optimized scenario that take your business to the next level.

We first work to understand the essence of your needs taking your environment, background, corporate culture, and incentives into consideration. Then we place importance on delivering results designed to best leverage your competitive strengths. Our consultants provide comprehensive and extensive support to offer practical solutions with no risk of straying from reality and no perspective bias.

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