Biostatistics
Standard Clinical Trial Timelines: A Sponsor’s Guide to Evaluating Biometrics CROs
This brief guide provides timeline benchmarks for Sponsors evaluating biometrics contract research organizations (CROs).
Clinical Trial Design: Ensuring Statistical Validity and Identifying Consulting Biostatisticians
Why engage a biostatistician early in the study design process, and how do you identify the right consultant for your study?
Statistical Support for Regulatory Submissions and Confidently Navigating Regulatory Discussions
How can an experienced biostatistician provide critical support before and during the regulatory submission process?
Key Interactions Between Biometrics Teams for a More Efficient Clinical Trial
Discover key interactions between clinical data management and biostatistics teams for a more efficient clinical trial.
Meet the PharPoint Team: Carson M., Biostatistics Manager
Learn more about what makes working at PharPoint Research unique and get to know biostatistics manager Carson M.
The Journey of Clinical Trial Data Points: From Patient to TLFs
Learn more about the journey clinical trial data takes before ending up on the package insert of a drug you’re taking.
Key Components for Ensuring Quality Statistical Output
How do our experts produce quality statistical analyses? Proper planning, processes & review are critical.
Adaptive Trial Design and the CRO Landscape
Learn more about the shifting CRO landscape, as PharPoint’s manager of programming technologies discusses adaptive trial design and outsourcing with EDC provider Medrio.
How and When to Consider a Data Monitoring Committee
How and when should you consider a DMC (also known as a DSMB, DSMC, or IDMC)? Learn more in this brief video.