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CPCC Co., Ltd.
Booth No. 1-023
Building Strong Evidence Through Clinical Trials
Drawing on insights gained from managing over 800 clinical trials, we propose the optimal trial design tailored to your needs. We provide comprehensive support throughout the entire process from initial study planning, protocol development, study management, data aggregation, statistical analysis, report preparation, and the drafting and submission on research papers.
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Clinical trial services

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Presentaion
Date 12:00 12:05~ Location PA
Title Directly linked to results! Trial design that maximizes the value of intestinal environment evaluation
Detail Evaluating the gut environment in human clinical trials involves many invisible obstacles that affect outcomes. This joint seminar provides insights from two expert companies, covering everything from result-driven, reliable study design to tips for smooth trial operation. Discover the practical processes that will lead you to acquire high-value evidence. We look forward to seeing you at the venue!
Date 12:30 12:35~ Location PB
Title New trends in intestinal environment research: From short-chain fatty acids to beyond - Human clinical trials that expand possibilities
Detail Unveiling new trends in gut microbiome research: moving beyond Short-Chain Fatty Acids (SCFAs). This seminar introduces the latest insights into gut environment evaluation, highlighting the importance of comprehensively analyzing metabolites like amino acids alongside SCFAs. What is the next-generation human clinical trial design that differentiates you from competitors? Join us to explore new possibilities for building robust evidence.
Date 15:30 15:35~ Location PA
Title Characteristics, Assessment Methods, and Challenges of Frailty (Psychological and Physiological) in Middle-Aged and Older Adults
Detail In 2014, the concept of frailty was proposed, and interest in methods for evaluating and improving frailty has been growing. However, efforts to prevent and improve frailty are still insufficient. Therefore, in this lecture, I would like to provide an overview of frailty, as well as discuss its actual conditions surveys, evaluation methods, and the challenges facing these issues.
Date 16:00 16:05~ Location PA
Title Evaluation methods for trials without clinic visits and their challenges
Detail In this seminar, we will discuss key considerations for assessment methods and operational challenges in decentralized clinical trials (DCTs). Topics will include approaches to obtaining subjective and objective study data, the online informed consent process, and the use of daily diaries to capture longitudinal participant-reported data.

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