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    The Total Economic Impact of TransPerfect GlobalLink for Life Sciences

    resource

    TransPerfect commissioned Forrester Consulting to conduct a Total Economic Impact™ (TEI) study and examine the return on investment (ROI) enterprises may realize by deploying GlobalLink. The objective of the framework is to identify the cost, benefit, flexibility, and...

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    • Medical Device - MDR - IVDRMedical Device Localization: Navigating Compliance and Empowering Engagement
    • Content Management - CCMS/SCMS/DMSScaling Clinical and Regulatory Content with GlobalLink's Intelligent Performance
    • Clinical Outcome Assessments - COA - eCOAThe Role of AI and Machine Learning in Clinical Outcome Assessment Translation
    • Medical AffairsPrepared, Not Overbuilt: How Smart Life Sciences Organizations Set Themselves Up for Commercialization, Global Partnerships, Licensing, and IPOs
    • Digital - Localization, SEO, Patient RecruitmentYour Multilingual Trial Site SEO Success Checklist
    • Why Global Medical Affairs Can’t Ignore Website Localization
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Blog

Leveraging Social Media for Patient Recruitment in Clinical Trials

Blog

The Quality Review of Documents (QRD) v9.0 for Veterinarians: A Step Toward Better Care

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Centralizing Global Content Solutions for Medical Affairs

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What Are Unitary Patents and What Do They Mean for Life Sciences Companies?

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Centralizing Global Content Solutions for Patient Engagement Teams

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Overcoming 5 Challenges of Implementing eClinical Technologies

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The C3 Summit: San Francisco Recap

Marketing & Sales Solutions

Over 30 years supporting marketing and sales teams across the life sciences industry build strategic campaigns to effectively reach consumers globally....

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The C3 Summit: Boston Recap

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The Future of eCOA and Wearable Devices

Medical Affairs

Streamline your medical affairs operations with TransPerfect’s complete suite of content solutions. Achieve omnichannel engagement with your med affairs content. ...

Contact - Service Highlight

Blog

The Role of Qualitative Interviews in Ensuring a Patient-Centered Approach to Clinical Trials

Education Hub

TransPerfect Medical Device Solutions is the first supplier to combine ISO 13485, 14971, and 9001 certified, patented language services with validated process automation technologies to meet the content management challenges of evolving regulations....

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Navigating the Regulatory Landscape for Expanded Access Programs

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Driving Success in Omnichannel Content Strategies for Global and Local Markets

Trial Master File Solutions

Interpretation

LMK Clinical Research Consulting

Event Apr 20, 2023

C3 Summit San Francisco

Join your industry peers for Conversations on Clinical Content, C3 Summit. Panels of pharma, biotech, CRO, and regulatory thought leaders will explore patient diversity, centricity, and outcome assessments, discussing challenges, opportunities, and strategies through the lens of real-world experience. Take away practical insights and participate in a discussion during the Q&A and post-event cocktail hour. ...

Event Sep 24, 2024

C3 Summit Princeton 2024

Join your industry peers for Conversations on Clinical Content, C3 Summit. Panels of pharma, biotech, CRO, and regulatory thought leaders will explore patient diversity, centricity, and outcome assessments, discussing challenges, opportunities, and strategies through the lens of real-world experience. Take away practical insights and participate in a discussion during the Q&A and post-event cocktail hour. ...

Event Oct 19, 2023

C3 Summit Princeton

Join your industry peers for Conversations on Clinical Content, C3 Summit. Panels of pharma, biotech, CRO, and regulatory thought leaders will explore patient diversity, centricity, and outcome assessments, discussing challenges, opportunities, and strategies through the lens of real-world experience. Take away practical insights and participate in a discussion during the Q&A and post-event cocktail hour. ...

Event May 16, 2023

C3 Summit Boston

Join your industry peers for Conversations on Clinical Content, C3 Summit. Panels of pharma, biotech, CRO, and regulatory thought leaders will explore patient diversity, centricity, and outcome assessments, discussing challenges, opportunities, and strategies through the lens of real-world experience. Take away practical insights and participate in a discussion during the Q&A and post-event cocktail hour. ...

Event Sep 13, 2023

C3 Summit London

Join your industry peers for Conversations on Clinical Content, C3 Summit. Panels of pharma, biotech, CRO, and regulatory thought leaders will explore patient diversity, centricity, and outcome assessments, discussing challenges, opportunities, and strategies through the lens of real-world experience. Take away practical insights and participate in a discussion during the Q&A and post-event cocktail hour. ...

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