The 2023 Clinflash Connect Annual Conference was successfully concluded
Clinflash Connect Annual Conference.
On December 21st, the 2023 "Digital Intelligence Driven Insight into the Future" Clinflash Connect Annual Conference organized by EDC was held in Shanghai. This event invited more than 10 important guests to conduct multi-angle discussions on the practical application and development trend of digital technology in the field of clinical trials.
In this event,Nearly 200Elites in the pharmaceutical R&D industry came to the scene to have in-depth exchanges with the guests1300 bitsThe audience shared digital innovation achievements through online participation, and worked with EDC to promote the digital development of pharmaceutical R&D.
Wonderful review of the morninghighlights review—am
Theme: Joining hands with EDC to drive the process of pharmaceutical innovation through digitalization.
Speaker: Guan Weihua, General Manager of EDIC
At the beginning of the conference, Mr. Guan Weihua, general manager of EDS, first delivered a speech, introducing the current development of clinical trial digitalization in detail to the participants, and further emphasizing the vision and mission of EDS. In the future, EDC will continue to adhere to the concept of "working with customers to achieve excellence" and provide professional clinical trial digital solutions and related services for the majority of pharmaceutical colleagues.
Topic: The history and future prospects of ClinFlash system.
Speaker: Li Ji, Deputy General Manager and Head of R&D Department
Mr. Li Ji, deputy general manager and head of the R&D department of EDC, introduced the development history, application and future development direction of the CLINFLASH series system in detail to the audience present and live broadcast, and pointed out that EDC will continue to pay attention to the needs of users and the cutting-edge direction of the industry, constantly update and iterate the system functions, and efficiently help the development of various clinical trials.
Topic: Digital Intelligence Tools to Improve the Efficiency and Quality of Clinical Trials.
Speaker: Prof. Yao Chen, Director of the Department of Statistics, Peking University First Hospital, Deputy Director of Clinical Research, Peking University, and Vice President of Hainan Real World Data Institute
Professor Yao Chen, Director of the Statistics Office of Peking University First Hospital, Deputy Director of Clinical Research of Peking University, and Vice President of Hainan Real World Data Research Institute, demonstrated the practical direction and development prospects of digital intelligence tools in clinical trials from different modules such as regulatory development, practical value, academic research, and case sharing, and encouraged more clinical trial participants to adopt digital intelligence technology to promote trial development.
Topic: How to use an all-in-one platform to efficiently run clinical trials.
Speaker: Liang Kong, Vice President of Clinical Operations of LaNova Therapeutics
From the perspective of clinical operations, Mr. Kong Liang, Vice President of Clinical Operations of LaNova, showed the audience the various problems faced by clinical operations in China, and explained in detail how to use the integrated platform with CTMS as the core to efficiently manage the whole process of clinical operations.
Topic: Exploration and Application of Decentralized Clinical Trials.
Speaker: Jiaojiao Yu, Head of DCT Solutions at Tigermed
From the perspective of decentralized clinical trials, which has attracted much attention in recent years, Yu Jiaojiao, head of DCT solutions, explained the specific concepts, regulatory development process, important breakthroughs, digital applications and other contents of DCT to the audience on site and live broadcast, so that many trial participants have a deeper understanding of this new trial model.
Roundtable Discussion: Application Practices and Challenges of Digital Clinical Trials
At the end of the morning session, the above-mentioned speakers gathered at the roundtable forum to share their challenges and suggestions for the current digital application of clinical trials.
Wonderful review of the afternoon
highlights review—pm
Topic: Visualization Tools in Clinical Trials.
Speaker: Guo Wenran, head of the data intelligence application team of CSPC Pharmaceutical Group
Ms. Guo Wenran, head of the data intelligence application team of CSPC, introduced how to use visualization tools to improve the all-round management of clinical trials and improve the efficiency of clinical research by explaining the advantages of data visualization, data standardization, data automation, etc.
Roundtable Forum: Construction and Application of Clinical Trial Data Warehouse.
Speaker: Miao Yadong, Director of Clinical Data Department, Clinical Center, CT Tianqing Research Institute
Mr. Miao Yadong, Director of the Clinical Data Department of the Clinical Center of CT Tianqing Research Institute, took the evolution of the data management work model as the starting point, showed the practical application of clinical trial data warehouse through the explanation of data warehouse solutions and the introduction of multiple data warehouse application scenario cases, and depicted the future development direction of data warehouse with actual work requirements.
Topic: Medidra Medical Coding & Application Recommendations.
Speaker: MSSO Medical Officer Dr. Chen Junchao
Dr. Junchao Chen, Medical Officer of MSSO, gave a detailed introduction to the application of Meddra, the key points to consider in MedDRA and the best practices of Meddra, providing guidance and help for the audience to use Meddra effectively in their work in the future.
Topic: Application and Practice of ECO in Patient-Centered Clinical Trials.
Speaker: Xue Yanbang, Solution Manager of EDCI
Based on the concept of "patient-centered", which has attracted the attention of all parties in the industry, Xue Yanbang, Solution Manager of EDIC, shared the relevant regulations of ECOA, the practical value of ECO and the application cases of ECOA, to help more audiences further understand the significance and value of electronic clinical outcome assessment.
Topic: Challenges and Practices of IRT Use in Innovative Experimental Design
Speaker: Dr. Wenjie Wang, Senior Biostatistics Manager of EDC
On the basis of sharing the basic concepts of randomization and management system, Dr. Wenjie Wang, Senior Biostatistics Manager of EDC, combined with the challenges and innovative design of the IRT system in combination with the current ever-changing trial design, further demonstrated the current requirements of the IRT that needs to be realized, and pointed out the importance of the IRT system in clinical trials.
Topic: Statistical Model-Based Data Review Design and Optimization
Speaker: Li Qi, Director of Data Management of Yingen Biotech
Ms. Li Qi, Director of Data Management of Yingen Biotech, introduced the key points of data quality consideration (data entry, questioning, source data verification, protocol deviation risk verification) and data volume consideration points (enrollment progress, subject distribution) in detail, to help the audience fully understand the detailed rules that need to be paid attention to in the design and optimization of data review.
Topic: Experience sharing on efficient CAR-T data management in EDC.
Speaker: Lujia Zhang, Senior Manager of Data Management at JW Therapeutics
Lujia Zhang, Senior Manager of Data Management of JW Therapeutics, gave a detailed analysis of the matters that need to be paid attention to in data management of CAR-T projects by introducing the process and characteristics of CAR-T projects, the considerations of database construction and data cleaning.
Topic: Applications and Challenges of Digital PV Databases in Clinical Trials.
Speaker: Xu Bin, head of EDC pharmacovigilance database
As an indispensable part of clinical trials, pharmacovigilance is gaining more attention from trial participants, Xu Bin, head of Medici pharmacovigilance database, clarified the importance of digital technology in pharmacovigilance by introducing the development process of pharmacovigilance regulations and the challenges faced by the current pharmacovigilance work, and shared his views on the future development direction of pharmacovigilance.
Topic: How to efficiently manage the documentation of the clinical trial process.
Speaker: Bo Wang, Head of CTA of Tigermed
On the basis of introducing the importance and regulatory requirements of clinical trial documents, Bo Wang, the head of CTA of Tigermed, further expounded the advantages of digital technology in the management of clinical trial documents based on the practical application of Clinflash ETMF, and put forward effective suggestions for the management of clinical trial documents.
Digital Achievement Showcase
achievement display
With the rise of ChatGPT, more and more trial participants have begun to pay attention to the application of artificial intelligence technology in clinical trials. Keeping up with the forefront of technology, EDC has long been promoting the development of artificial intelligence in the field of clinical research digitalization, and will show it to the on-site participants during this conferenceAI auto-coding function, received praise and recognition from many guests.
Wonderful moments of the conference
conference moments
Although the 2023 Clinflash Connect Annual Conference has come to an end, the pace of pharmaceutical innovation will never stop. As an industry leader in clinical research cloud solutions and related professional services, EDC is well aware that digitalization is an important development direction for pharmaceutical R&D, and is committed to communicating and exchanging with more partners through various activities.
In the future, we will cooperate with the majority of pharmaceutical colleagues in a more diversified way to empower the pharmaceutical R&D process with leading digital technology, and look forward to seeing you at more events next year!Special blessings
Pros
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