How Chinese CRO, Zhejiang Longcharm Biomedical Technology Uses Pinnacle 21 Enterprise to Optimize Sponsors’ Non-clinical and Clinical Regulatory Affairs Case Study 中国 CRO 浙江龙传生物医药科技有限公司如何使用 Pinnacle 21 Enterprise 优化申办方的非临床和临床法规事务 Learn how one CRO uses Pinnacle 21 to optimize sponsors’ clinical regulatory affairs, saving time…Certara2024 年 5 月 6 日
为什么临床数据标准对 EDC 和 Non-EDC 数据至关重要? 博客 为什么临床数据标准对 EDC 和 Non-EDC 数据至关重要? 临床数据标准对 EDC 与 non-EDC 数据均至关重要。Learn how study build…Certara2024 年 4 月 25 日
Pinnacle 21 Releases New PMDA, FDA, NMPA Validation Engines Announcement Pinnacle 21 Releases New PMDA, FDA, NMPA Validation Engines Pinnacle 21 by Certara announces the latest Validation Engines for submissions to Japan PMDA, US…Certara2024 年 4 月 23 日
CRF Design Checklist Guide CRF 设计核对表 Our free, downloadable CRF design checklist can help you design quality case report forms that…Certara2024 年 4 月 10 日
临床元数据存储库应该做些什么? 博客 临床元数据存储库应该做什么? 2024 年 4 月 4 日 As the clinical research industry moves towards more efficient and automated processes, clinical…Certara2024 年 4 月 4 日
How Clinical Trial Software Helps Make Studies More Efficient Blog 临床试验软件如何帮助提高研究效率 2024 年 3 月 13 日 Clinical trials play a crucial role in advancing medical research and improving…Certara2024 年 3 月 13 日
Clinical Data Standardization: Achieving Cleaner Data and Faster Regulatory Submissions On-Demand Webinar Clinical Data Standardization: Achieving Cleaner Data and Faster Regulatory Submissions Master the essentials of clinical data standardization for regulatory submissions in this best practice webinar:…Certara2024 年 1 月 16 日
SEND Dataset Quality Control: Best Practices & Recommendations Blog SEND Dataset Quality Control: Best Practices & Recommendations In this blog, Senior Product Management Director Peggy Zorn explores best practices & recommendations for…Certara2023 年 4 月 25 日
New FDA Validator Rules V1.6 Explained Blog New FDA Validator Rules V1.6 Explained In this blog, we explore what you need to know about the update to the…Certara2023 年 1 月 12 日