Grow Your Team's Capabilities with Global Learning Content

The technical and instructional design expertise to create, deploy, and translate engaging training content that edcucates your global teams.

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Learning design for the life sciences industry

Effective learning design is essential for training global teams and audiences on the latest scientific developments, technologies, and regulations. Whether it's developing courses for researchers, clinicians, regulatory professionals, or other stakeholders, the learning materials need to be tailored to local cultures and languages.

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Our Training and Development Solutions for Life Sciences

Content Development

Work with in-house, life sciences content authoring experts who can create training modules using all major file formats, e-learning authoring tools, and learning platforms, ultimately saving you 40% in costs.

Course Localization & Adaption

Provide courses in your employee's native language with expert translation and adaptation services. TransPerfect localizes courses for maximum retention and cultural appropriateness.

Voiceover & Subtitling

Create e-learning videos from concept inception to script writing to production to release. Adapt your content with voiceovers and AI-driven subtitling workflows.  

Testing & Quality Assurance

Rest assured that your training materials will be void of image display errors, incorrect links, video timing issues, and more. Our QA testing process ensures your global audience consumes the best possible content.

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Managed In-Country Review

Manage shared content among multiple authors, reviewers, and quality assurance experts, while also incorporating a terminology glossary and translation memory to capture all the work to reuse in future projects. 

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Simultaneous Interpretation

For investigator meetings or large, diverse gatherings, TransPerfect provides interpretations of two or more languages at the same time to engage global audiences in their native languages.  

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TI GlobalLearn

TransPerfect Life Sciences offers the Trial Interactive Learning Management System (TI Global Learn), providing organizations with a web-based, compliance-focused learning and training solution with flexible configurability and intuitive reporting for easy oversight. All of Trial Interactive’s modules are 21 CFR Part 11 compliant.

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The Power of Partnering in Training & Development

The Power of Partnering with a Global Content Team

TransPerfect provides training support across any platform, in 200+ languages, and any subject matter. Our team centralizes your global learning requirements and manages the administrative work, so you can roll out your content quickly and cost-effectively.

Multilingual e-Learning Content Your Team Will Remember and Use

Train all staff working in the development of a product—internal staff, consultants, CROs, investigators, study staff and more—in their native language. Know the content will be remembered and used to avoid protocol deviations. Document the training to maintain data quality.

Better e-Learning by the Numbers

50 k+

Training projects launched

40 %

Savings with centralized global learning and development

50 %

Faster content releases

TransPerfect supports Pfizer in the development of the Global Learning Program: Partner4Better

Pfizer needed to develop an online learning portal to support the HCPs they engage with across the globe, with a particular focus on emerging markets. The content they produced needed to be accessible, engaging, and in line with Pfizer’s overall mission to improve global health equity.

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.

Global Training for Protocol, Regulatory & SOP Compliance

When developing and commercializing life sciences products that are governed by global regulatory agencies, the smallest misstep can result in major problems. Proper training and documentation helps to keep your clinical research on track. 

News and Thought Leadership

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

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 ...

Improve content retention and compliance with global regulations

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