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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

    Things to Consider When Shipping Internationally

    by Hope Cullen October 3, 2013
    written by Hope Cullen

    As industry professionals, we spend a lot of time and energy writing, designing and producing materials in support of clinical trials. During this process, shipping materials to their final destination is often an afterthought, with address information provided at the last minute. This is not such a big deal when materials are shipped domestically. But lack of planning can derail a carefully calculated timeline when shipping internationally. Arming yourself with information can mean the difference between getting materials to a site in time for a site initiation visit and missing the deadline completely. When preparing to ship internationally, knowing the following will help minimize delays and missed dates.

    1. Some countries have value limitations. Shipments have a value. Your manufacturer or fulfillment partner will ship materials at the same value you purchased them. Some countries cap the value of shipments and, when exceeded, a more formal (and longer) customs clearance process must occur. Knowing this will allow you to plan your shipments. Do you break them into smaller shipments over time to stay under the limit? Do you send one large shipment and plan for the longer customs process, so you ultimately get the materials to their destination on time?

    2. Most international shipments require an importer of record. This is a person or company with an import license in the destination country that can assist with clearing a shipment through customs. If you are shipping to your company’s satellite office or a partner company, it is likely they will have an import license and all is well. However, if you want to ship direct to a destination that does not have an import license, you must have an importer of record to assist with customs clearance. When shipping direct to sites or hotels for investigator meetings, these destinations often do not have, or will not use, their import license for your materials. In this event, you need an alternative. This is easy for companies that have offices in different countries. If you do not have an in-country office that can act as the importer of record, you need to find someone who can assist, or take your chances. Planning ahead can make a big difference.

    3. Some countries require additional information. Details such as tax ID’s, CUIT’s, CNPJ’s, etc., are required to import materials. Knowing destination requirements in advance helps minimize the last-minute scramble for information that can be difficult to acquire quickly.

    4. Some items require additional information. Often customs offices want to know where the items were manufactured, what the items comprise (textiles, metal, etc.), and other details. The more information you know in advance the better. A shipment that is in transit can be delayed as you hunt down and obtain manufacturing information and conformity certificates.

    If I can offer any advice of value, it is this: For international shipments, plan your shipping methodology in advance, and ensure you have a fulfillment/logistics partner that is knowledgeable about international customs. These two things will help keep your timeline intact, and keep you and your company in compliance.

    Happy shipping!

    October 3, 2013 0 comments
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  • Participant Engagement

    What’s in a Name? The Power of Study Branding

    by Felicia Fuller September 9, 2013
    by Felicia Fuller September 9, 2013

    Early in my tenure with DAC Patient Recruitment Services, back when we were D. Anderson & Company, we presented a proposal defense to a pharmaceutical company that was sponsoring a study aimed at a particular ethnic group. The sponsor needed help creating a patient recruitment …

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  • Clinical Trial Business Insights

    Lost Art of Face-to-Face Meetings

    by Melynda Geurts August 23, 2013
    by Melynda Geurts August 23, 2013

    Physiologically speaking, a mental picture is worth a thousand words. So, isn’t it interesting that we’ve taken a social society by nature and applied modern technology to make business practices more efficient? And yet, we are skeptical of individuals who choose not to post their …

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  • Translation of Clinical Trial Materials

    Can You Differentiate in Translation?

    by Brandon Bissell July 8, 2013
    by Brandon Bissell July 8, 2013

    The question of value differentiators in the translation industry is important to translation buyers and translation providers alike. With thousands of translation companies vying for increasingly competitive opportunities, and increasingly experienced and skeptical clients moving beyond the benchmark questions of quality and timelines, it’s essential …

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  • Participant Engagement

    Recruitment & Retention – Getting Specialized

    by Melynda Geurts May 16, 2013
    by Melynda Geurts May 16, 2013

    Worldwide patient recruitment continues to be the most predominant reason clinical trials fall behind projected enrollment goals. Industry sources say that for every day a drug is delayed to market it can cost the company anywhere from $1M to $8M a day. What if you could …

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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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