Improve Outcomes with Diverse Datasets

Scalable and secure data collection, annotation, and chatbot translation services.

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Translations Memory Life Sci

Deploy high-performance AI products to improve patients’ quality of life

Life sciences organizations continue to amass enormous amounts of unstructured data sets. The complexity of these vast collections of data can prevent sponsors and other clinical companies from accessing operational and patient efficiencies offered by machine learning.

TransPerfect Life Sciences' AI/ML data services resolve the complexity and enable machine learning models by converting unstructured data to structured data, combining highly efficient human input with state-of-the-art tools and workflows so that the result is accurate and unbiased.

HIPAA-Compliant Data Collection and Annotation Built for Scale

Ensure better-balanced datasets across 200+ languages with our data collection and annotation services, without breaking the bank. Our labeling team is comprised of ground truth experts, meaning all data provided comes by direct observation/measurement. From audio to video and images to text, our platform provides a scalable content moderation solution in secure facilities on the cloud.

Chatbot Localization

An estimated 80% of standard queries can be answered by chatbots. Our end-to-end chatbot localization service ensures your stakeholders receive accurate, fast responses in their native language through collecting global patient prompts; categorizing said prompts into groups; and then running user tests for compliance, conceptual equivalence, and cultural appropriateness.

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The Latest Developments in Artificial Intelligence for Life Sciences

Benefits of our AI Platform, DataForce

  • Stronger, global, diverse datasets
  • Recruiting large volumes of resources at scale
  • Up to 80% reduction in timelines
  • Flexible integration capabilities with our platform or third party of your choice
  • Up to 1,000 annotators onboarded within weeks of project kick-off
  • Compliant with SSAE 16 SOC 2, ISO 27001, HIPAA, & GDPR

Enhance Internal Efficiencies While Improving Patients' Quality of Life

For data scientists, machine learning engineers, and product managers looking to deploy high-performance AI products in the healthcare industry, DataForce by TransPerfect is a market leader in scalable and secure data collection and annotation services. DataForce converts unstructured data to structured data, combining highly efficient human input with state-of-the-art tools and workflows so that the result is accurate and unbiased to ensure companies are at the front line of innovation in bringing treatments and solutions to the world.

News and Thought Leadership

Our subject-matter experts have in-depth understanding of the technological challenges, requirements, and goals for life sciences organizations.

The C3 Summit: Boston Recap

The second event in our series of C3 Summits took place in Boston on May 16, 2023. We invited industry experts and leaders to discuss challenges, opportunities, and strategies in clinical trial diversity, centricity, and outcome assessments through the lens of real-world experience. In this recap of the Boston session, we will review key points from each session.  Session 1: COA/eCOA Innovations – Licensing Hiccups, Linguistic Validation, ePRO Migration, and Best ...

The C3 Summit: Boston Recap

How Medical Writing Can Drive Patient Engagement

Medical writing is a critical component of the broader patient engagement landscape, establishing the foundations of communication between pharmaceutical companies and patients. The quality of medical communication can be transformational in how a patient engages with and...

A Conversation with Dr. Elin Haf Davies of Aparito

The rare disease space presents numerous challenges for clinical research and patient data capture. These challenges are only heightened for younger patient populations, where outcome measures and dosages need to be considered appropriately. Join Dr. Elin Haf Davies, Founder & ...

Navigating the EU Clinical Trial Regulation Complexities - Current Challenges and Opportunities

As the most significant change in the European Union clinical trial legislative ecosystem in 20 years, the European Union Clinical Trial Regulation 536/2014 (EU CTR) went live on January 31, 2022. The first-year transition period has now ended, and from January 31, 2023, EU ...

How to Maximise Value and Avoid Failure During Life Sciences Dealmaking

Please complete the form below to access the on-demand recording of our webinar. A fantastic expert panel of life sciences dealmaking veterans from AstraZeneca and Merck, with 100 years' collective experience, share their insights on key dealmaking strategies, best practices ...

Centralizing Global Content Solutions for Medical Affairs

With a rapidly evolving landscape and the introduction of new technologies and emerging therapeutics, medical affairs professionals are tasked with remaining in lockstep with the latest industry developments. From a content perspective, this means not only maintaining clear...

Automation for MDR & IVDR: A Three-Part Seminar - Part 3: EnCompass Step by Step: A Detailed View of the Content Automation Solution to Meet MDR & IVDR Requirements

Part 3: EnCompass Step by Step: A Detailed View of the Content Automation Solution to Meet MDR & IVDR Requirements ...

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