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Meet Melisa Williamson, Director of Quality Assurance
Get to know PharPoint's new Director of Quality Assurance, Melisa Williamson, with a quick Q&A ...
How to Create a Comprehensive Clinical Development Strategy
A strategic clinical development plan (CDP) can help Sponsors optimize their new drug programs. What should you include in your CDP? ...
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75+ free resources from PharPoint | Insight, checklists, & more
CRO Study Team Continuity and Transparency
Will you actually be working with the team a CRO introduces you to in early discussions? ...
Case Study: Proactive Risk Mitigation in Early Phase Oncology
This case study highlights how the PharPoint team supported a Phase 1 FIH oncology study that completed LPLV and database ...
Meet Melisa Williamson, Director of Quality Assurance
Get to know PharPoint's new Director of Quality Assurance, Melisa Williamson, with a quick Q&A ...
Considerations for Sponsors Conducting Protocol Feasibility and Review
A comprehensive protocol review requires a multi-disciplinary group. Who should be included and what should this group be looking for? ...
Clinical Trial Budget Risks: The Hidden Cost of Protocol Amendments
Protocol amendments are increasingly common. What are they costing you? ...
Achieving Expedited Database Lock with Director of DM, Wendy Moffett
Director of Data Management Wendy Moffett discusses how PharPoint achieves rapid database lock in this short video ...
Contract Research Organizations 101: What is a CRO?
What does a CRO do? Go back to basics with us ...
Effective Site Feasibility: It all Starts with a Protocol and a Question(naire)
Learn what goes into an effective site feasibility questionnaire and how an experienced consultant can help inform your strategy ...
No Surprises: PharPoint’s Transparent Approach to Changes in Scope
How does your CRO handle changes in scope (CIS)? Learn more about PharPoint's transparent process ...
