CDISC SEND Updates Nonclinical Drug Developers Need to Know
In this blog, Peggy Zorn explores updates to the Standard for Exchange of Nonclinical Data…
CertaraApril 6, 2026
From Documentation to Design: Building a Scalable Metadata Strategy for Clinical Research
Learn how clinical teams are treating metadata as infrastructure to improve reuse, auditability, and standards…
CertaraFebruary 26, 2026
Metatdata as Infrastructure: Designing for Reuse, Insight, and Auditability
Watch this on-demand webinar to learn how leading clinical teams design scalable metadata strategies that…
CertaraFebruary 26, 2026
P21 Enterprise Expands Regulatory Validation Capabilities with Support for the Tobacco Implementation Guide v1.0
Pinnacle 21 supports TIG v1.0, the CDISC Tobacco Implementation Guide for FDA CTP, enabling automated…
CertaraJanuary 30, 2026
How to build standardized eCRFs across multiple EDC systems
Discover how to build standardized eCRFs across multiple EDC systems to improve data quality, accelerate…
CertaraDecember 12, 2025
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
