Biostatistics

Randomization: An Introduction to Methods and Technology

Learn more about common methods and technology options available to support your trial’s randomization needs.

July 25, 2024
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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?

July 3, 2024
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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?

June 27, 2024
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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.

June 18, 2024
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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.

February 29, 2024
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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.

March 9, 2021
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Key Components for Ensuring Quality Statistical Output

How do our experts produce quality statistical analyses? Proper planning, processes & review are critical.

December 1, 2020
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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.

October 9, 2019
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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.

October 9, 2016
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