クリオサイエンスは抗がん剤の開発、医師主導治験などのオーハン薬開発などを通じ、世界中の人々の健康と福祉に貢献する育薬ベンチャーです。

Clio Science Inc. serves the development of new drugs and medical devices as a contract research organization (CRO). Our strengths are in oncology, cardiovascular and central nervous system (CNS).
We offer our professionally skilled monitors to your organization and guarantee a high quality result.

Inquiries to principal investigators and clinical trial sites
Making contracts with clinical trial sites
Delivery and collection of investigating drugs
Monitoring
Collecting and checking Case Report Forms (CRF)
Source Document Verification (SDV)
Termination procedure of clinical trials

Verification of essential documents
Verification of monitoring reports
Development of Standard Operating Procedure (SOP) for quality control
Verification of clinical trial related activities
Verification of evaluated work in Safety Information
Storage management of data

Monitoring
Collecting and checking Case Report Forms (CRF)
Source Document Verification (SDV)

Development of SOP for quality control, based on GQP, GVP and QMS
Consultation no Pharmaceutical Affairs
Support on Pharmaceutical Affairs audit

Our staff includes people who have experience in the medical industry and CRO business, backgrounds in medicine, veterinary science, pharmacy and nursing. They also attended 250 hours of training to become reliable and responsible CRAs.
Employee training includes manner, GCP, general knowledge of medicine and science, followed by continuous assessments on a regular bases.

At Clio Science Inc., we encourage our staff to participate in a lifelong study. Not only to improve their pharmaceutical knowledge and ability in trouble solving, but also to enhance their qualities as a CRA. In order to support this, we provide more than 50 hours of training classes a year.