是什么促使对 SEND 数据集服务的需求增加？ Blog Post
Gain an understanding of CDISC SEND dataset creation challenges impacting the biopharma industry, and how these factors could delay regulatory submissions and strategic initiatives.
Closing the Loop: How to Improve the Management of Your Design-Make-Test-Analyze Cycle Blog Post
在快速发展的医药领域，小分子药物的研发不仅是一项科学挑战，也是对项目管理和信息整合能力的严峻考验。The right technology streamlines the drug discovery…
Certara.AI Blog Post
Transcript: Did you know that eighty percent of life sciences data is unstructured? This data is messy, difficult to search, often resides in silos. Having unstructured data means that you…
Certara Talks: PHUSE 2024 Recap Blog Post
In this episode of Certara Talks, Jeff Abolafia, Kristin Kelly, and Julie Ann Hood recap their fantastic presentations from PHUSE US Connect earlier this month. The team covered inspirational and…
Precision Predictions: Simcyp™ Simulator for Kinase Inhibitors Blog Post
Transcript:In pharmaceutical research and development, R&D, companies utilize biosimulation and PBPK modeling technologies to identify and develop new therapeutic agents. Biosimulation technology holds immense potential for expediting FDA approvals while…
Validation Page
Pinnacle 21Pinnacle 21 Enterprise: De-risk and expedite submissions by ensuring clinical data compliance Learn more about our clinical data validation engine Book a demoCommunity resources Ensure your clinical data is...
Don’t Miss Our Inaugural Event for Biosimulation Users Blog Post
Join us for an in-person event where you can learn from drug development experts, network with peers, and discover the latest trends and best practices in biosimulation.
Everything You Need to Know About CRFs in Clinical Trials Blog Post
了解 CRF 与 eCRF 设计基础知识、为何应标准化注释 CRF 及云端 CRF 软件的优势。
PBPK for Drug-Drug Interactions (DDI) Blog Post
This white paper introduces PBPK modeling as a vital tool for accurate DDI prediction, showcasing its role in expediting drug approval.
