Simplify Your Path From Lab to Launch

Navigate Life Sciences complexities with industry-leading global content solutions and specialized services.

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Driving Your Patient-Centric Mission Forward

TransPerfect Life Sciences supports your clinical journey from site identification to product launch. 

Streamline regulated clinical trial work streams to expedite timelines and accelerate therapeutic breakthroughs.

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Ensure the success and compliance of your breakthrough therapeutics in the global marketplace.

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Protect and manage intellectual property, streamline global HR operations, and provide support solutions to power your global corporate operations.

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COA & eCOA

Ensure conceptual equivalence and cultural appropriateness in any language, minimizing time-to-market, mitigating risk, and ensuring regulatory compliance in global studies.

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Regulatory Solutions

Clear regulatory hurdles with consulting and content solutions and accelerate your approval process. Avoid missteps in translations, labeling, or packaging that lead to regulatory findings post-filing. Complete global submissions in a timely fashion. 

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PV & Safety Solutions

Observe, detect, and monitor the effects of your pharmaceutical products across locations and languages with translation and call services. Ensure drug safety across your entire portfolio.

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eClinical Solutions

Support your clinical research and trials with TransPerfect Life Sciences’ eClinical technology, Trial Interactive. Trial Interactive is an industry leader in practical, global eClinical innovation that simplifies and automates clinical processes for sponsors, CROs, and sites around the world. 

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Medical Device Solutions

TransPerfect Medical Device Solutions (MDS) is the medical device industry’s largest provider of translation services and content automation technology. Learn how you can reduce the cost, risk, and turnaround time of new MDR and IVDR content requirements by 50%—and effectively translate/localize your website, app, software, e-learning, and other digital content.

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Translation Services

Meet multilingual challenges of document translation with powerful technology and expert linguist support to alleviate manual project management burdens associated with the translation process.

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Structured Content Authoring

Increase content reuse by 50% with TransPerfect’s Component Content Management System (CCMS). Reuse content, propagate changes, enable omnichannel delivery, and streamline the review and approval process to reduce cycle time and costs.

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Call Center Support

Customize call center support to meet your goals. Our services combine innovative technology, fast-speed service, and customer-focused care. Our team supports call center launches, supplements existing call center resources, handles overflow call volume, and provides over-the-phone interpretations services.

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Trusted by Life Sciences Organizations Big and Small

Syneos Health
Gilead
Boehringer Ingelheim
Vertex
Alexion
St Jude Medical
Allergan
AstraZeneca
Biogen
BMS
Chiesi
Clario
CVS Health
Evidera/PPD
Fulgent
Hologic
ICON
Innovaderm
IQVIA
Johnson & Johnson logo
Labcorp
Bayer
Merck
MGH

Join TransPerfect’s community of more than 1,000 life sciences organizations, including pharma, biotech, meddev, CROs, and IRBs.

"Thank you so much for your attention on Pfizer drug approval. This study was inspected very smoothly with your efficient translation support during the inspection period last month! The approval of IBRANCE in China was absolutely great news for Chinese patients."

"Without the collaboration of the TransPerfect team, we wouldn’t be able to get materials to market as quickly and efficiently as we do today. TransPerfect is saving our internal partners extraordinary time and effort. A major reason for this program’s success has been the collaboration; our contact at TransPerfect is consultative, listening closely to our business problems and offering meaningful solutions. The TransPerfect team has been fantastic to work with."

"When I think of TransPerfect, I think of Disneyland. TransPerfect makes dreams come true."

"Before GlobalLink for AEM, we had to manage translation processes outside AEM, adding an extra layer of processes and approval flows into our work stream. Now it all happens within the same system, making translation and approval flows smoother."

"Thank you so much for the expedited turnaround and for helping us get this accomplished. Signant Health appreciates everything TransPerfect does for us! Your team is the best."

"I am delighted with our collaboration. TransPerfect accurately and effectively briefed the interpreters, leading to smooth, engaging, and respectful conversations with patients and their caregivers. This, indeed, had a positive influence on the outcomes."

"With Trial Interactive, we help studies lower risk and achieve near real-time oversight, without site visits."

"Trial Interactive has without question improved ARCA’s ability to complete trials in the most efficient manner possible."

"Trial Interactive was the most robust for Karyopharm’s global use. Plus, we have access to other Trial Interactive’s other integrated modules as we evolve our process."

"When I think of TransPerfect, I think of Disneyland. TransPerfect makes dreams come true."

"TransPerfect supported us on building a great learning experience for our community. Elements of gaming like point scoring and competition with others are incorporated in a training to learn our KPI definitions and targets."

"TransPerfect supports Shire’s Medical Information team with the regionalization of response documents. Their high-quality medical writing and translation support team has enabled us to get critical information to physicians faster—helping us achieve our goal to help our patients lead better lives."

"Without the collaboration of the TransPerfect team, we wouldn’t be able to get materials to market as quickly and efficiently as we do today."

"Trial Interactive provides an important combination of IT and service solutions for a growing company: a scalable eTMF packaged with implementation, validation, management, and oversight services."

"Trial Interactive has been key to enabling us to perform remote monitoring visits."

News and Thought Leadership

Explore recent events and learn more about happenings at TransPerfect Life Sciences.

LifeSci Talks | From Interview to Endpoint: Understanding the Importance of Patient Listening to Build Better Outcomes

In this episode of TransPerfect LifeSci Talks, Mark Wade, Global Practice Leader at TransPerfect Life Sciences sits down with John Reites, Co-Founder and CEO of THREAD research to discuss the importance of patient listening to build better clinical trial endpoints. They delve into the differences between enterprise and standalone solutions, challenges with standardization, and the influence of evolving technologies in the eCOA industry. ...

LifeSci Talks | From Interview to Endpoint: Understanding the Importance of Patient Listening to Build Better Outcomes

Transcreation in Clinical Research: How to Use Transcreation and Localization to Resonate with Your Audience

Clinical teams need to communicate with multilingual audiences across the globe while also meeting strict regulatory requirements. In addition to helping teams remain compliant, accurate translations ensure the highest standards of patient safety are met across clinical...

Where to Apply Machine Translation in Life Sciences Content Workstreams Right Now

In the life sciences industry, it’s increasingly essential to reduce cycle times and enhance operational efficiencies, especially across clinical and commercial team processes. To address evolving regulations from global health authorities and the common pain points of costs,...

The Imperative of Accurate Translations in Clinical Research

With the increase of global clinical trials, clinical documentation is required to be accurately translated at every stage from lab to launch. Despite the administrative burdens and tight regulatory timelines that clinical teams face, accuracy cannot be sacrificed in life...

How Pharmacovigilance Automation Solutions Can Help You Meet Tight Regulatory Reporting Timelines

Pharmacovigilance (PV) teams play a critical role in detecting, assessing, understanding, and preventing the unintended adverse effects of medications and treatments. Their work, which includes drug reaction monitoring, drug safety surveillance, side effect monitoring,...

How to Improve the Speed and Accuracy of Patient Communications in Clinical Development

According to Phesi, more than a quarter of clinical trials conducted in 2023 were canceled during Phase II.  As clinical research teams struggle with patient recruitment and engagement under tight deadlines and immense regulatory pressure, patients also grapple with...

Implications of AI in Healthcare and Life Sciences: Ethical Considerations in the Age of AI

Artificial intelligence (AI) models have already shown transformative potential in the life sciences industry, including automating administrative clinical research tasks, analyzing patient data to predict future health risks, synthesizing medical information, and more. ...

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