Certara Products - Pinnacle 21 Archives

Blog

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…

Certara2025 年 12 月 10 日

Conference

2025 MFDS-KCDA Annual Conference

Certara2025 年 11 月 20 日

Conference

PHUSE APAC Connect 2026

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Certara2025 年 11 月 20 日

Webinar

Modern SDTM Starts Here: Metadata Management with P21 Enterprise Plus

Certara2025 年 11 月 13 日

Case Study

Validation in clinical data management: MacroGenics® Optimizes Validation and Issue Management with Pinnacle 21® Enterprise

Discover how MacroGenics optimized validation in their clinical data management with our centralized, collaborative Pinnacle…

Certara2025 年 11 月 12 日

Blog

How To Design a Case Report Form | 7 Best Practice Steps

Discover how to design a case report form with our 7 best practices: improve data…

Certara2025 年 11 月 3 日

Fact Sheet

CRF Creator Fact Sheet

Learn how Pinnacle 21 CRF Creator streamlines CRF design and build, enabling more efficient study…

Certara2025 年 10 月 28 日

Video

Pinnacle 21 Enterprise Plus: Your Route to Faster, Compliant SDTM Mapping Specs

Automate SDTM data transformation with Pinnacle 21 Enterprise Plus mapping specification software, and automatically comply…

Certara2025 年 10 月 24 日

On-Demand Webinar

The Impact of Standardized eCRFs from Data Collection to Submission

Certara2025 年 9 月 16 日

Case Study

Biogen 利用 Certara 元数据管理重构临床研究管理

Discover how study metadata management, paired with CDISC standards, transformed Biogen’s clinical trial processes and…

Certara2025 年 9 月 5 日

Certara Products – Pinnacle 21