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    Clinical Trial Business InsightsClinical Trial Materials Development and Printing

    International Clinical Trial Printing: Think Globally and Print Regionally

    by Ted Corrigan October 8, 2024
    written by Ted Corrigan

    Get highlights on how the international clinical trial printing vendor you select can impact everything from timelines to sustainability.

    Imperial supports numerous studies by writing, translating, designing, and printing clinical trial materials for sponsors, CROs, clinical research sites, and research patients. For this blog post, I will focus on how the printing vendor you select can impact your worldwide study.

    Printed materials are important and impactful tools that have proven necessary for conducting clinical research studies worldwide. These materials are often used in unison with digital-based tools such as websites, videos, social media campaigns, and study apps. Printed materials are continuously rolling off Imperial’s presses in the United States and the United Kingdom, destined for sites and participants across the globe.

    The selection of a printing vendor is actually a strategic one.

    Speed saves more than time

    I spoke with Dan McDonald, Imperial vice president of business development. He gave examples of the benefits of using an international clinical trial printing vendor like Imperial. “Speed is definitely an advantage,” he said. “While most pivotal clinical trials are global in scope, the majority of study sites are in North America and Europe. Being able to print and distribute closer to the sites in those regions shaves significant time off the time-to-site metric. This also eliminates the expenses and logistics concerns of shipping overseas.”

    Greater flexibility

    Dan also mentioned Imperial’s print-on-demand feature, which brings great flexibility to study timelines. “By printing materials nearer to the final destination, we can narrow the window of how early we have to receive the client files for printing and finishing before they are needed on site,” he said. “This just-in-time form of printing allows us to customize materials for specific countries and take that burden away from in-country teams.” 

    Sustainability

    Sustainability is very important to Imperial as well as our clients, and Dan pointed to the advantages of using international companies like Imperial. “We lower our clients’ carbon footprint by printing materials closer to their end destination. That eliminates the tremendous amount of energy required to move materials across the world by plane.”

    Logistics expertise

    Even though printing regionally means you’re utilizing sources closer to the materials’ destinations, logistics concerns about moving from one country to another still play a role. Frankie Bentley, Imperial associate director, touted the logistics advantages of using an international clinical trial printing vendor like Imperial. “Our U.S. and U.K. subject matter experts are logistics specialists with decades of country-specific experience adhering to regulations and customs requirements and navigating the many potential pitfalls that come with getting materials to sites.”

    The Imperial advantage: Uniform quality and expertise plus best-in-class customer service

    Imperial’s U.S. and U.K. experts work seamlessly within a single organization, driven by standardized processes and a robust quality management system. This brings uniform excellence across all of our service lines.

    Frankie Bentley added, “Whilst we diligently adhere to all the minute details regarding regulations and customs requirements, we never lose sight of our company’s dedication to exceeding expectations. Our focus is always on providing a best-in-class, truly customer-centric experience.”

    October 8, 2024 0 comments
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  • Clinical Trial Materials Development and PrintingParticipant Engagement

    Tips for a Patient-Friendly Clinical Trial Informed Consent Form

    by William McEwen September 25, 2024
    by William McEwen September 25, 2024

    A patient-friendly informed consent form (ICF) is a key element for prospective clinical trial participants’ understanding of a clinical research study. In this blog, we delve into tips to ensure the ICF is clear and understandable. The research ICF document provides potential participants with the …

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  • Clinical Trial Materials Development and PrintingParticipant Engagement

    Long-Term Clinical Trial Participation: 6 Tips to Retain and Keep Patients Engaged

    by Kori Ammon September 12, 2024
    by Kori Ammon September 12, 2024

    Retaining participants in studies is an ongoing challenge that the clinical trials industry grapples with daily. One analysis1  I came across pegged the participant dropout rate at an average of 25-26 percent per study. Every single loss is costly and, among other problems, can prolong …

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  • Clinical Trial Business Insights

    Mastering Clinical Trial Timelines

    by Heather Ross August 20, 2024
    by Heather Ross August 20, 2024

    Realistic, well-managed clinical trial timelines are essential to the success and timeliness of clinical studies. Read on for more information about keeping your projects on track. We often say every clinical trial is made up of a million moving parts. The materials, equipment, and supplies …

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  • Clinical Trial Materials Development and PrintingParticipant Engagement

    Writing Clinical Study Materials: Connect with Patients and Professionals

    by William McEwen August 6, 2024
    by William McEwen August 6, 2024

    Whether you’re a sponsor, CRO, or part of a study team, writing clinical study materials that resonate with your audience is crucial for recruitment, referrals, and retention. Our tips will get you started and guide you through the writing process. You know all the standard …

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  • Clinical Trial Materials Development and PrintingParticipant EngagementTranslation of Clinical Trial Materials

    Clinical Research Translation: Can You Manage all the Moving Parts?

    by Heather Ross May 2, 2024
    by Heather Ross May 2, 2024

    Clinical research translation affects almost every global study. Understanding the translation process and the planning required can help keep your study on track. Clinical trial statistics can be surprising. We frequently write about different aspects of the growing complexity of global clinical trials. Despite the …

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  • Clinical Trial Business Insights

    3 Tips to Make Your Clinical Trial Teams Agile and Proactive

    by Ted Corrigan March 6, 2024
    by Ted Corrigan March 6, 2024

    Clinical trial teams must be agile and proactive in the evolving world of clinical studies. Research teams navigating today’s dynamic landscape face a multitude of risks due to the ever-increasing pace of change. These risks can include: Technological advances rapidly rendering initial plans obsolete Supply …

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  • Ancillary Clinical Trial Supplies and EquipmentClinical Trial Materials Development and PrintingParticipant Engagement

    6 Top Picks: Clinical Trial Blogs Not to Miss

    by William McEwen December 27, 2023
    by William McEwen December 27, 2023

    The Imperial blog team took a look at our 2023 clinical trial blogs, and we’re shining the spotlight on our top six picks. So here they are, in no particular order: six clinical trial blogs worth reading (and re-reading). 1. Supply Chain: Master these key …

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  • Participant Engagement

    3 Tips to Avoid the Holiday Season Impacting Participant Compliance

    by Heather Ross December 13, 2023
    by Heather Ross December 13, 2023

    We often refer to participants as the heroes of research. Clinical trials and the medical advances made through research don’t happen without them. But here comes the holidays – will your study participant compliance waver during these busy times? Patient recruitment, retention, and compliance with …

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  • Translation of Clinical Trial Materials

    Clinical Trial Translation: Precision Is Key

    by Erica Manning May 9, 2023
    by Erica Manning May 9, 2023

    Accurate clinical trial translation services are key to the overall success of a study. Each participant needs to receive the same information in their native language to ensure consistent study messaging across all languages and accuracy to the protocol. I’ve compiled key translation best practices …

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Imperial Clinical Research Services Blog

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