Certara Products - Pinnacle 21 Archives

Announcement

Certara Introduces CRF Creator Module in Pinnacle 21® Enterprise for Faster Clinical Study Start-Up in Drug Development

Discover Pinnacle 21® Enterprise Plus' new CRF Creator module, designed to speed clinical study start-up…

Certara2026 年 2 月 6 日

Blog

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…

Certara2026 年 1 月 30 日

Blog

How to build standardized eCRFs across multiple EDC systems

Discover how to build standardized eCRFs across multiple EDC systems to improve data quality, accelerate…

Certara2025 年 12 月 12 日

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…

Gilbert Hunter2025 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

On-Demand Webinar

Modern SDTM Starts Here: Metadata Management with P21 Enterprise Plus

Discover how P21 Enterprise Plus modernizes SDTM metadata management for efficiency, consistency, and compliance across…

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

Certara Products – Pinnacle 21

Certara Introduces CRF Creator Module in Pinnacle 21® Enterprise for Faster Clinical Study Start-Up in Drug Development

P21 Enterprise Expands Regulatory Validation Capabilities with Support for the Tobacco Implementation Guide v1.0

How to build standardized eCRFs across multiple EDC systems

7 key annotated CRF regulatory submission requirements you should know

2025 MFDS-KCDA Annual Conference

PHUSE APAC Connect 2026

Modern SDTM Starts Here: Metadata Management with P21 Enterprise Plus

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

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

CRF Creator Fact Sheet

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