Everything You Need to Know About CRFs in Clinical Trials
Read about the basics of CRFs and eCRF design, why annotated CRFs should be standardized…
Certara2024年3月26日
The State of AI in In Silico Trials and Drug Development – The Practical Application of AI in QSP [APAC Webinar]
The proliferation of AI models and GPTs has revolutionized how the life sciences industry consumes…
Danielle Pillsbury2024年3月20日
Adding Quality Control & Validation to Drug Discovery with AI
The proliferation of powerful AI models, including GPTs, has revolutionized how the life sciences industry…
Danielle Pillsbury2024年3月14日
How Clinical Trial Software Helps Make Studies More Efficient
2024年3月13日 Clinical trials play a crucial role in advancing medical research and improving…
Certara2024年3月13日
Everything You Need to Know About SDTM
Find out all you need to know about CDISC SDTM, from the SDTM implementation guide…
Certara2024年3月12日
Best Practices for a Successful eCTD Submission
Learn common pitfalls that pharmaceutical sponsors encounter during the regulatory eCTD submission procedure and best…
Certara2024年3月5日
What is new in Phoenix 8.5?
Phoenix8.5の最新バージョンで追加された新機能と強化された機能について、Watch the webinar to learn…
Danielle Pillsbury2024年2月26日
Guide to development of compound files for PBPK modeling in the Simcyp population-based simulator
The Simcyp Simulator is a software platform for population physiologically-based pharmacokinetic (PBPK) modeling and simulation.…
Jim Gallagher2024年2月23日
Streamlining Your NCA Workflow
PK analysis intended for submission contends with many data and compliance challenges. To work efficiently,…
Danielle Pillsbury2024年1月18日
Higher Standards: Achieving Cleaner Data, Faster, from Protocol to Submission
Join our webinar to explore best practices for harnessing the power of standards, without a…
Danielle Pillsbury2024年1月16日
