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Clinical Trial Materials Development and Printing Participant Engagement Translation of Clinical Trial Materials

3 Steps to Create User-Friendly Participant Materials

by Marta Korgol September 9, 2026
Clinical Trial Business Insights

Rethinking Diversity Through Inclusive Clinical Trial Design

by Vaughn X. Anthony September 2, 2026
Clinical Trial Business Insights Clinical Trial Materials Development and Printing Translation of Clinical Trial Materials

How Version Control in Clinical Trial Materials Reduces Risk

by Heather Ross August 26, 2026
Ancillary Clinical Trial Supplies and Equipment

Why Ancillary Supplies Are Rarely Ancillary in Clinical Trials

by Imogen Cheese August 4, 2026
Ancillary Clinical Trial Supplies and Equipment Clinical Trial Business Insights Clinical Trial Materials Development and Printing

Vendor Consolidation in Clinical Trials: Why It Matters

by Dan McDonald July 21, 2026
Clinical Trial Business Insights Participant Engagement Translation of Clinical Trial Materials

Translation vs. Localization in Clinical Trials: Why the Difference Matters

by Sian Lukaszewicz July 15, 2026
Clinical Trial Materials Development and Printing Participant Engagement

Designing Clinical Trial Materials Older Participants Can Navigate with Confidence

by Vaughn X. Anthony June 2, 2026
Clinical Trial Business Insights Participant Engagement

Celebrating Clinical Trials Day: From a Shipboard Study Site to Today

by William McEwen May 20, 2026
Ancillary Clinical Trial Supplies and Equipment Clinical Trial Business Insights

Why Ancillary Supplies Are Becoming a Critical Part of Clinical Trial Planning

by Dan McDonald May 19, 2026
Clinical Trial Materials Development and Printing

Writing Clinical Study Materials: Why Starting Early Can Be an Option

by Liz Wegner May 6, 2026
  • Study & Site Print Materials

  • Ancillary Trial Supplies

  • Translation Services

  • Trial Patient Engagement

    Participant Engagement

    3 Limitations of Databases for Patient Recruitment

    by Melynda Geurts May 11, 2015
    written by Melynda Geurts

    Not too long ago, online communities became a popular alternative to the low volume of referrals and inaccuracy of traditional media. These communities began as central hubs where patients gathered online to discuss their illness and seek knowledge or support.

    As the industry came to realize the powerful capabilities of these communities, pharmaceutical companies quickly began building their own online centers in hopes of building a large, mineable database for their own clinical trial recruitment projects. These databases take years to build, but can evolve into very large and powerful information centers.

    Although these databases have brought enormous advantages to clinical trial recruitment, there are severe limitations to this strategy.

     

    3 Limitations of Databases for Patient Recruitment

     

    1. Demographics Grow Out-of-Date

    Certain demographic data are reliable and permanent, for example birth date or race. However, a significant portion of demographic data can grow out-of-date very quickly and result in inaccurate referrals by the time the data are used to recruit for a trial. Individuals may no longer have the time or ability to commit to the protocol requirements, or they may no longer meet the required criteria.
    Some examples of soon-to-be-outdated demographic characteristics include:

    • Physical characteristics such as weight or pregnancy status
    • Geographic location, address, phone number
    • Life situations, married, student, job change

    2.Medications Grow Out-of-Date

    Similar to certain demographic data, medication information can quickly become outdated in databases.  Recruiting patients based on their medication history as it appears in the database leaves room for the possibility that they may have added different medication or changed dosage since the time of data entry. Wasted efforts in recruiting subjects who no longer fit the criteria will add up quickly and prove to be costly.

    3.Cost

    Databases are extremely costly to develop and maintain. In order to maintain a reliable database, one must overcome the previous two challenges by keeping the data up-to-date and accurate. This requires a significant amount of resources and manpower. Continuous effort must be made to connect with patients and other data sources. This is not to mention the resources required to construct the database, such as manpower, hardware, software, and other costs.

    To learn more about the limitations of internally-generated database strategies and what you can do to leverage existing and fluid communities, grab a copy of our recent ebook here!

    May 11, 2015 0 comments
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  • Clinical Trial Business Insights

    Imperial Expands Global Footprint with UK Acquisition

    by Steve Swanson April 30, 2015
    by Steve Swanson April 30, 2015

      Global studies are the norm, more often than not in this day and age. As this trend continues, so too must the infrastructure development and the global footprint of companies that support clinical trials. As of April 2015, Imperial has acquired Four Point Printing …

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  • Translation of Clinical Trial Materials

    A Checklist for Preparing Your Next Translation Project

    by Erica Manning April 27, 2015
    by Erica Manning April 27, 2015

    You’ve spent weeks leading a team of people who have invested countless hours of time, energy, emotion and resources creating your patient materials.  The text was drafted and then laid out into the carefully chosen study design.  Round upon round of painstaking review commenced. Finally, …

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  • Participant Engagement

    Modern Patient Recruitment – How Did We Get Here?

    by Melynda Geurts April 13, 2015
    by Melynda Geurts April 13, 2015

    In recent years, a plethora of new patient recruitment tactics have surfaced that take advantage of new technology. Over the last two decades, the industry has gone from relying on personal physician referrals to highly advanced and proactive solutions. Although problems with patient recruitment continue …

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  • Clinical Trial Business Insights

    Outsourcing in Clinical Trials Southeast 2015

    by Maria Anderson April 3, 2015
    by Maria Anderson April 3, 2015

    The 4th Annual Outsourcing in Clinical Trials Southeast conference was recently held at the Embassy Suites in Cary, North Carolina on March 24-25th.  This conference provided a unique platform for discussion alongside case-study-led presentations delivered by virtual, small and large Pharma/Biotech and Medical Device perspectives. …

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