Supporting Patient Diversity in Clinical Trials

Patient diversity, equity, and inclusion (DEI) in clinical trials is an important focus for both regulatory authorities and other industry stakeholders. Diverse participants in clinical trials can help us understand how treatments work in populations — particularly those who are most impacted by a disease.

 

A Collaborative, Unified Approach

PharPoint is committed to seeking opportunities for people from all backgrounds, especially those who are typically underrepresented in clinical trials, to participate in and benefit from clinical research. PharPoint strives to promote diversity and equity through our site feasibility and selection processes as well as patient outreach and support services.

We cultivate a unified approach alongside our Sponsors and Sites that promotes a collaborative team focused on the common goal of recruiting and retaining diverse populations that are impacted by the targeted disease.

 

 

Some of the ways we support this approach include:

  • Site selection with purpose: Identifying sites and principal investigators who can help meet trial diversity goals, including the selection of sites in geographical areas with access to target patient populations
  • Tools and technology to improve access: Leveraging tools and technology that can increase accessibility, such as helping Sponsors incorporate home or telehealth options
  • Planning with DEI in mind: Inclusion of DEI topics in the discussion of site-specific recruitment plans, such as ensuring representative populations are shown in patient-facing materials

 

PDF DOWNLOAD Supporting Patient Diversity in Clinical Trials  

About PharPoint

PharPoint Research is a consultative contract research organization (CRO) that helps innovative sponsors meet their study goals. For more information about PharPoint and our services, reach out to our team.


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EBOOK

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).


Exploring Standard CRO Timeline Benchmarks

Preparing to work with a top biometrics contract research organization and wondering how their promised data management, biostatistics, and medical writing timelines match up to the industry average? To help sponsors dig into these details and ensure the timelines they’re receiving are competitive, we’re providing PharPoint’s typical timelines alongside research that calculates industry standard timelines, when available.

Our hope is that this document can help sponsors set realistic expectations, confidently ask the right questions of their vendors, and ultimately, partner with a top biometrics CRO that keeps their study moving: because patients are waiting.

 

eBook contents include:

PharPoint’s short eBook, Standard Clinical Trial Timelines: A Sponsor’s Guide to Evaluating Biometrics CROs, includes the below information.

  • Standard database build timeline
    • The bigger picture: Considering site identification and study start-up
  • Standard mid-study database change timeline
  • Standard database lock time
    • Six strategies for a faster database lock
  • Evaluating database lock to top line results timeline
    • Ensuring a rapid delivery
  • Evaluating database lock to delivery of tables, listings, and figures (TLF) timeline
  • Standard clinical study report delivery timeline
  • About PharPoint Research

Compare Standard Clinical Trial Timelines

For instant access to the eBook, fill out the form below.


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