Simplify the Creation, Release, and Management of Multilingual Content

Reduce your cycle times and translation costs while improving resource allocation and achieving greater visibility

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Drive Consistency and Transparency with GlobalLink TMS

TransPerfect’s translation management system (TMS) helps leading life sciences organizations:

  • Icon Automate Manual Processes

Automate manual tasks

  • Icon Magnifying Glass with a Clock

Ensure a comprehensive audit trail, including a clear record of who made changes and when they were made

  • Icon Checklist 2

Facilitate a collaborative online review process to eliminate the need for an email with marked-up files

  • Icon AI Integrations

Centrally manage and leverage translation memory (TM) and other linguistic assets

  • Icon Data

Capture important data for reporting and KPI metrics

  • Icon Network 2

Integrate with other content repositories

Centralize your content in a web-based, intuitive, and secure platform

Streamlining processes to reduce cycle times and increase efficiency is an increasing trend within the life sciences industry. TransPerfect’s enabling translation technology platform, GlobalLink, automates manual steps, drives consistency through central translation memories (TMs) and linguistic assets, incorporates machine translation (MT) workflows, and offers real-time reporting for greater visibility and control. GlobalLink TMS streamlines the translation process and provides standardization that can accelerate the time-to-market by 40–60% and decrease translation costs by 25–40%.

GlobalLink TMS at a Glance

6 k+

Clients trust GlobalLink

50 %

Reduction in translation costs

40 %

Reduction in cycle times

50 %

Reduction of internal project management and IT dependencies

50 +

Out-of-the-box connectors for automation

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GxP and CFR 21 Part 11 compliant

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Key partnerships, including Veeva and Adobe

GlobalLink

Translation Management Technology That Supports Your Growth

Sponsors supporting global operations produce vast amounts of content in need of translation. The complexity of content volume, tight timelines, quality and compliance concerns, administrative burden, and budget constraints all challenge the efficiency of managing content translation at scale.

TransPerfect Life Sciences' TMS solutions help sponsors navigate content complexities by driving process automation, improving TM efficacy and consistency, incorporating MT workflows, and optimizing content review to shorten cycle times and reduce total translation costs.

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News and Press Releases

Our industry experts have in-depth understanding of the challenges, requirements, and goals for life sciences organizations involved in clinical trial management.

Fast, Compliant, Centralized Translation in Action: Lessons from AbbVie & Immunovant

Due to high interest following our GlobalLink NEXT panel, we’re welcoming back Stacey Higgins, Associate Director, COA & Digital Implementation Team of AbbVie alongside Tihirah Harris, Sr Manager, Clinical Business Operations of Immunovant to share how and why they moved to a centralized, tech-enabled translation model—enabling faster trial timelines, cost control, and regulator-ready content. We'll also cover what’s ahead on their centralization roadmap, ...

Fast, Compliant, Centralized Translation in Action: Lessons from AbbVie & Immunovant
Blog

How Patients Discover Clinical Trial Websites: The Role of Localization in Search and Trust

Could localization be the key to improving patient recruitment in clinical trials?Recruiting participants for clinical trials is a critical step in bringing new therapies and treatments to market, but despite advances in digital outreach, the industry still faces major...
Webinar

LifeSci Talks COA Series | Modernizing eCOA: Emulators, Backups, and the Future of Reporting

In this tech-forward episode of LifeSci Talks, Mark Wade, Global Practice Leader at TransPerfect Life Sciences, welcomes Indira Jain-Figueroa, Product Director at Evinova, for a deep dive into the ever-evolving landscape of eCOA development. Covering everything from cross ...
Blog

Rewriting the Rules of Informed Consent Development with AI

How AI and Structured Content Management Are Transforming the ICF ProcessInformed consent forms (ICFs) are essential to clinical trials, serving as the primary vehicle for communicating study information to participants in a clear, ethical, and compliant manner. Given...
White Paper

Could Data Standardizations be the Silver Bullet for Faster Electronic Clinical Outcome Assessment (eCOA) Deployment?

Choosing an electronic clinical outcome assessment (eCOA) provider is a complex process that involves a variety of different aspects including experience, scientific support and knowledge, integration capabilities, scalability, study-specific requirements, and so much more. ...
White Paper

Accelerating Pharma Labeling with Intelligent, Compliant Content

Juggling multilingual labels across varying regions and products? Managing the updates and complying with local health authorities' requirements can be a challenge for global pharmaceutical companies, who are facing increasing pressure to streamline labelling processes and ...
Webinar

Engaging Patient Communities: A Pathway to Clinical Trial Success

In this webinar, expert speakers from MTS Sickle Cell Foundation, Inc, Rare Disease Diversity Coalition, Black Women’s Health Imperative, and Clinical Research Associates, Inc. will focus on the critical role of patient communities in advancing clinical trials. They will ...

Learn Why Leading Life Sciences Organizations Love GlobalLink TMS

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