How one university overcame practical and cultural challenges to implement CDISC compliance Case Study 一所大学是如何克服实际操作和文化挑战来实施 CDISC 合规性的 A US-based university with a nationally recognized academic health center implemented Clinical Data Interchange Standards…Certara2024 年 5 月 8 日
A Best Practice Guide to CDISC SDTM Mapping Guide CDISC SDTM 映射最佳实践指南 Complete the form to book your no-obligation demo of Pinnacle 21 and experience the transformative…Certara2024 年 5 月 7 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
The State of AI in In Silico Trials and Drug Development – The Practical Application of AI in QSP [APAC Webinar] On-Demand Webinar AI 在虚拟试验与药物研发中的新篇章:QSP 的实际应用探索【亚太地区网络讲座】 The proliferation of AI models and GPTs has revolutionized how the life sciences industry consumes…Certara2024 年 3 月 20 日
Adding Quality Control & Validation to Drug Discovery with AI On-Demand Webinar Adding Quality Control & Validation to Drug Discovery with AI The proliferation of powerful AI models, including GPTs, has revolutionized how the life sciences industry…Certara2024 年 3 月 14 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
Best Practices for a Successful eCTD Submission Blog 成功递交 eCTD 的最佳做法 Learn common pitfalls that pharmaceutical sponsors encounter during the regulatory eCTD submission procedure and best…Certara2024 年 3 月 5 日