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.
Define-XML Page
Pinnacle 21Define-XML: Automate your Define.xml files with Pinnacle 21 Learn more about automating Define-XML Book a demo todaySupport and resources Have your define.xml files ready to submit faster Define.xml is...
How Clinical Trial Software Helps Make Studies More Efficient Blog Post
Steven Benham March 13, 2024 Clinical trials play a crucial role in advancing medical research and improving patient outcomes. The effectiveness of studies relies heavily on cutting-edge technology to optimize...
Everything You Need to Know About SDTM Blog Post
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.
Best Practices for a Successful eCTD Submission Blog Post
Learn common pitfalls that pharmaceutical sponsors encounter during the regulatory eCTD submission procedure and best practices for addressing them.
CERTAINTY by Certara 2024 | Teaser Blog Post
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…
Dose Optimization Considerations for Targeted Radiation Therapies Blog Post
The acquisitions of targeted radiation therapy companies (TRT) Point Biopharma by Eli Lilly and RayzeBio by Bristol Meyer Squibb have sparked investors’ interest in this therapeutic class. A growing number…
Phuse US Connect Blog Post
Conference: Phuse US Connect Date: March 16-19, 2025 Location: Orlando, Florida Booth: A Sponsor: Platinum Meet us there Where to hear Certara insights and Expertise Monday, March 17, 4:30-5pm ET...
Bridging the Gap: Integrating Pharmacometrics with Quantitative Systems Pharmacology (QSP) for Smoother Clinical Phase Transitions Blog Post
Master clinical phase transitions with insights from industry leaders! Join Piet van der Graaf, SVP and Head of QSP, Hugo Geerts, Head of Neuroscience Modeling QSP, Mirjam Trame, VP of…
Incorporating Pragmatic Elements in Study Designs to Enhance Oncology Randomized Clinical Trials Blog Post
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…
