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.

Trusted by Life Sciences Organizations Big and Small

Join TransPerfect's community of over 1,000 life sciences organizations, including pharma, biotech, CROs, IRBs, and agencies.

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Learn Why Leading Life Sciences Organizations Love GlobalLink TMS

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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.

Four Years In: What the EU Clinical Trial Regulation Has (and Hasn't) Delivered

When the EU Clinical Trial Regulation (EU CTR No 536/2014) went live for new submissions on January 31, 2022, it promised to transform how clinical trials are authorized and conducted across Europe: a single submission, one decision, and harmonized oversight. Four years in, the reality is more nuanced. The regulatory landscape, meanwhile, is moving faster than ever. In a recent Xtalks webinar, four subject matter experts with direct experience navigating CTR and ...

Four Years In: What the EU Clinical Trial Regulation Has (and Hasn't) Delivered

IMP Labeling Workflows That Reduce Relabeling Risk and Start-Up Delays

Investigational medicinal product (IMP) labeling sits at the heart of clinical trial supply, impacting departments across pharmaceutical organizations, from clinical operations and regulatory affairs to quality assurance and beyond. When labeling activities are managed across ...

The Missing Link: Why Study Design Makes or Breaks a Clinical Trial

In this episode of LifeSci Talks, Mark Wade, Global Practice Leader at TransPerfect Life Sciences, sits down with Farrell Healion, Founder and Principal Consultant at OptiTrial, to explore why study design is so often the overlooked "missing link" in clinical ...

C3 Summit 2026 - London

Conversations on Clinical Content, C3 Summit is part of a series of events hosted by TransPerfect Life Sciences featuring sessions with expert panels discussing present challenges, strategies, and innovations, as well as insights into future advancements, from R&D to ...

Considerations for eCOA in Global Clinical Trials

Regulatory Considerations for eCOA Submissions in Global Clinical Trials: What You Need to KnowWhen managing eCOA in clinical trials across multiple countries, translation, linguistic validation, and electronic implementation of Clinical Outcome Assessments (COAs) are...

Xtalks | EU Clinical Trial Regulation: Latest Developments and Upcoming Opportunities

The EU clinical trial landscape has changed significantly since Regulation (EU) No 536/2014 became applicable on January 31, 2022, and sponsors now need a clear view of how the framework is operating in practice and where it may evolve next. This webinar explores the current ...

Veeva RIM TMS Integration Checklist

If your regulatory team is still downloading documents from Veeva Vault, managing translation requests by email, or tracking submissions in spreadsheets, there's a better way. Reduce complexity, close compliance gaps, and shorten your submission cycle times with this ...