Define-XML Page
Pinnacle 21Define-XML: Automate your Define.xml files with Pinnacle 21 Learn more about automating Define-XML Book a demo todayCommunity resources Have your define.xml files ready to submit faster Define.xml is a...
The State of AI in In Silico Trials and Drug Development – The Practical Application of AI in QSP [APAC Webinar] Blog Post
人工智能模型和 GPTs 的普及彻底改变了生命科学行业消费信息和利用信息从而加速和验证研究的方式。By leveraging GPTs, researchers can complete…
SEND Dataset Services for FDA IND Submissions Page
灵活的 CDISC SEND 数据集创建与及时的质量审核服务，以支持 FDA IND 提交范围内非临床研究数据的提交。
Why Medical/Regulatory Writing Services Use Style Guides & Lexicons Blog Post
Learn how style guides and lexicons help medical writers produce clear, consistent, and accurate content for drug development and regulatory submissions.
Certara.AI: Real World Applications Page
Certara.AI Certara.AI: real world applications Accelerate submission timelines Meeting shrinking submission timelines while innovating faster on limited resources can feel overwhelming. That’s where CoAuthor, our GPT-powered regulatory writing platform, steps...
External Vendor Data Exchange Page
Pinnacle 21Streamline your external vendor data flow Learn more about Pinnacle 21 Enterprise Book a demo todayCommunity resources Get cleaner non-EDC vendor data, faster Pinnacle 21 Enterprise (P21E) revolutionizes the...
How Clinical Trial Software Helps Make Studies More Efficient Blog Post
Steven Benham 2024 年 3 月 13 日 Clinical trials play a crucial role in advancing medical research and improving patient outcomes. 研究的有效性在很大程度上依赖于前沿技术来优化和加速研究的构建和提交流程。 在本博客中，我们将介绍一些革新研究人员设计、管理和分析试验方式的创新软件解决方案。...
Everything You Need to Know About SDTM Blog Post
从 SDTM 实施指南到 SDTM 数据集创建的分步流程，了解有关 CDISC SDTM 的所有信息。
