7 key annotated CRF regulatory submission requirements you should know
Discover 7 key aCRF regulatory submission requirements for delivering high-quality annotated CRFs, including real-world examples…
Gilbert HunterDecember 10, 2025
QSP Workshop 2026 in Japan & Korea – Mastering Scalable AI-enabled QSP modeling software, Certara IQ™
Japan: February 26, 2026 - 1:00 - 5:00 pm | Korea: Wednesday, March 4, 2026…
CertaraDecember 9, 2025
On Virtual Twin® models in rare disease research, with Piet van der Graaf
Using Virtual Twin models in rare disease drug development can improve clinical trial design, regulatory…
CertaraDecember 9, 2025
Virtual triplets: The next step in personalized and ethical drug development
Learn how virtual triplets, linking PBPK, QSP, and organ-on-a-chip technologies, are transforming model-informed drug development,…
CertaraDecember 9, 2025
Changes to Our Long-Term Support (LTS) Release Schedule
Chemaxon's long-term support (LTS) release schedule changes starting January 1st, 2026.
CertaraDecember 9, 2025
Why Upgrade to Marvin? Unlocking Speed, Accuracy, and Scientific Intelligence
Watch this webinar to see how Marvin outperforms Marvin JS with faster chemical drawing, advanced…
CertaraDecember 8, 2025
Expedited Pharmacometrics Regulatory Submissions
Certara delivers complete, compliant pharmacometric regulatory submission packages in just 4–6 weeks, eliminating the PMx…
CertaraDecember 8, 2025
Therapeutic drug monitoring of amikacin in Chinese premature infant: a population pharmacokinetic analysis and dosage optimization.
See how PopPK modelling in Chinese premature infants identifies key covariates and supports model‑based amikacin…
CertaraDecember 6, 2025
PK Report Creation with AI: From Days to Minutes
AI PK Reports, a component of Phoenix Cloud, turns the protocol, data tables and figures…
CertaraDecember 4, 2025
