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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

    Clinical Trial Business Insights

    Timeline Management: In Search of the 25th Hour

    by Hope Cullen November 22, 2013
    written by Hope Cullen

    Do you ever feel there isn’t enough time in the day to get everything done? In the life-science industry, we are forever trying to achieve completion in time for the next site initiation visit or first patient in. Ensuring clinical trial materials are on-site in time can be challenging. To meet the challenge, it’s important to start with the end in mind.

    Knowing the first date materials need to be available provides the target. Using this, work backwards and add the activities involved in developing, producing and shipping materials, as well as the time required for each. In an ideal world, you would start with the end date, build in time to perform each activity, and come up with an appropriate start date. But let’s be honest, you may not have a lot of control over the start date, either.

    Start dates are typically dictated by protocol approval, purchase order initiation, or some other “go forward” activity. So take your ideal timeline and massage it to conform with the start and end dates. Though it can be much like trying to put 5 pounds of sugar into a 3-pound bag, by compressing, manipulating and maneuvering each activity’s time allotment you can often meet very aggressive deadlines.

    There are a few  things that can help you succeed. For projects with multiple components, such as medical writing, design, translation, printing, and shipment, choose a full-service provider that can perform all of these functions to maintain consistency in quality and control over timelines. At Imperial, we assign a project manager to oversee this process and to ensure communication occurs smoothly and with a level of transparency to our clients. The project manager also ensures accountability for activities so that internal team members and clients understand their roles and perform their assigned tasks on time to meet the ultimate target. By having an end-to-end understanding of all the steps and everyone’s role, the project manager helps to navigate the process forward to completion.

    Of course, sometimes a timeline just cannot be met. Two things no team should ever do is to skip steps or compromise quality to meet a deadline. While the need for speed is understandable, ultimately getting it right is more important than getting it fast. When circumstances conspire to make timelines unreachable, connect with your team and work through alternative solutions. Creative thinking and a sense of urgency helps to navigate what is sometimes an ever-moving target to support clinical trial needs.

    And sooner or later, maybe we can all find that 25th hour in the day.

    November 22, 2013 0 comments
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  • Participant Engagement

    Avoid These Top 5 Multicultural Marketing Mistakes

    by Felicia Fuller November 8, 2013
    by Felicia Fuller November 8, 2013

    The emergence of personalized medicine adds new complexity to patient recruitment, as clinical trial sponsors require participants to meet more granular criteria, including ethnicity. The challenge for drug development companies is to craft recruitment campaigns that educate, resonate and inspire communities of color to become …

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  • Clinical Trial Business Insights

    Site motivation. Want to learn more? Get closer.

    by Melynda Geurts October 25, 2013
    by Melynda Geurts October 25, 2013

    We’ve all heard these metrics — 31 percent of Phase 2 and 30 percent of Phase 3 trials are running longer. And site staff members are over-resourced. Time delays demotivate site performance. There are three pieces to the puzzle to make clinical trials successful, including pharmaceutical/biotechnology companies, …

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  • Clinical Trial Business Insights

    Site Solutions Summit: Reflections & Visions

    by Steve Swanson October 18, 2013
    by Steve Swanson October 18, 2013

    Having recently returned from this year’s Site Solutions Summit, it seems appropriate to share some reflections. Being on the Global Impact Partners Advisory Board for the Society for Clinical Research Sites (SCRS) provides a unique view into the planning and purpose of the summit. I can say …

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  • Participant Engagement

    5 Ways to Retain Patients Through Text Messaging

    by Vaughn X. Anthony October 11, 2013
    by Vaughn X. Anthony October 11, 2013

    Retention is the cornerstone of successful clinical trial completion; therefore, it is essential that subjects comply with study requirements, including visit schedules. Communication is key, and the easier the mode of communication, the better. That’s why text messaging has emerged as a convenient high-tech alternative …

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Imperial Clinical Research Services Blog

Imperial is a global leader in clinical trial solutions and support, specializing in study and site print materials, ancillary trial supplies and equipment, clinical trial translation management, and clinical trial patient engagement.

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