Featured resources
Operationalizing ICH E6(R3) and QbD with a Quality Assurance Consultant
How can a QA consultant help your team fully adopt QbD? ...
Key Components for Ensuring Quality Statistical Output
How do our experts produce quality statistical analyses? Proper planning, processes & review are critical ...
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75+ free resources from PharPoint | Insight, checklists, & more
Clinical Trial Database Design Process | Video
This short video takes a behind-the-scenes look at PharPoint's 6-8 week standard database build process ...
Clinical Trial Activity in Japan and Taiwan (2015-2025): Trends and Phase Distribution
A look at a decade of Phase 1-4 studies in Japan and Taiwan, from 2015 to 2025 according to ClinicalTrial.Gov ...
Research is Personal | Video
Clinical trials are both scientific and deeply personal. This short video reflects the perspective that guides our work in supporting ...
Preparing for ICH E6(R3): Understanding the 11 Core GCP Principles
Explore the 11 GCP principles outlined in ICH E6(R3) ...
Exploring Multiple Perspectives in Rare Disease Trials
What makes rare disease trials unique? Explore perspectives across functions from a rare disease CRO team ...
Database Build: Our Standard Timeline from Final Protocol to Database Go-Live
How long does it take to go from final protocol to database go-live? ...
Examining Strategies for Faster Clinical Study Report Timelines
Associate Director of Medical Writing Samia Khader explores a handful of strategies for expediting CSR delivery ...
Operationalizing ICH E6(R3) and QbD with a Quality Assurance Consultant
How can a QA consultant help your team fully adopt QbD? ...
Evaluating Quality Culture in Clinical Research
We spoke with PharPoint’s Director of Quality Assurance to explore what a “quality culture” in the clinical research space entails ...
