
Everything You Need to Know About CRFs in Clinical Trials Blog Post
Read about the basics of CRFs and eCRF design, why annotated CRFs should be standardized and the benefits of cloud-based CRF software.
Read about the basics of CRFs and eCRF design, why annotated CRFs should be standardized and the benefits of cloud-based CRF software.
Find out all you need to know about CDISC SDTM, from the SDTM implementation guide to a step-by-step process for SDTM dataset creation.
eCTD申請で陥りやすい落とし穴とは?製薬企業が知っておくべき課題とその回避策・対応に向けたベストプラクティスをご紹介します。
Transcript: The Certara community and interdisciplinary industry experts and scientists from model and form drug development bio simulation, clinical pharmacology, regulatory science, and software development come together for Certainty. Certara’s…
イーライリリーによるPoint Biopharma社、ブリストル・マイヤーズ スクイブによるRayzeBio社の買収により、標的放射線治療(TRT)という治療分野への投資家の関心が高まっています。A growing number…
業界の専門家の洞察を活用して、臨床フェーズの移行を完全に理解しましょう。Join Piet van der Graaf, SVP and Head of QSP, Hugo Geerts, Head of Neuroscience Modeling QSP, Mirjam Trame, VP of…
A FRIENDS OF CANCER RESEARCH WHITE PAPER The article explores the complex landscape of determining optimal drug doses in early-phase oncology trials, with a focus on achieving a delicate balance…