Commercialization Solutions to Effectively Reach Your Global Audiences

Choose precise and effective content solutions that keep your business compliant and your audiences well-informed throughout every step of the commercialization process. 

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Main Picture Commercialization

Solutions That Ensure Your Delicate Subject Matter Is Handled with Precision

Put your commercialization plan into action with an experienced partner who helps you create globally compliant content. 

Product Launch & Commercialization Regulatory Submissions Translation & Management Medical Affairs Content

Product Launch & Commercialization

Deliver important educational messaging about your product to healthcare providers and patients to ensure an effective global launch. Know that your product is positioned for success and patient safety with services such as digital marketing, culture consulting, literature and social media monitoring, and more.

  • Digital Marketing
    Digital Marketing
  • Multilingual Packaging
    Multicultural Marketing Consulting
  • Literature & Social Media
    Literature and Social Media Consulting
  • Website Localization
    Website Localization
  • SEO
    Search Engine Optimization
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Regulatory Submissions Translation & Management

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. 

  • Global Submission
    Global Submission
  • Multilingual Packaging
    Multilingual Packaging
  • Regulatory Consulting
    Regulatory Consulting
  • eCDT Support
    eCTD Support
  • Labeling Translation
    Labeling Translation
  • Alignment
    Labeling Alignment
  • Medical Writing 2
    Medical Writing
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Medical Affairs Content

Localize and manage medical affairs content through technology-backed workflows. Maintain cultural appropriateness and unbiased clinical and scientific messaging throughout your global marketplace.

  • Medical Writing
    Medical Writing
  • Translation
    Localization/Adaptation
  • Network 2
    Veeva Connector (MLR Workflows)
  • Document Management
    Content Reuse (SCMS)
  • Call Center
    Support & Customer Service
  • Chat
    Chatbots
  • AI Integrations
    AI Portal
  • Digital Marketing
    Digital Marketing
  • Literature & Social Media
    Literature and Social Media Monitoring
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Benefits of Choosing a Global Launch Partner by the Numbers

90 %

Reduction in project management burden

50 %

Faster customer response times

25 %

Saved on content development costs

35 %

Increase in contents’ perceived local quality

News and Thought Leadership

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

The C3 Summit: Boston Recap

Blog

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
Blog

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...
Webinar

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 & ...
Webinar

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 ...
Webinar

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 ...
Blog

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...
Webinar

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 ...

Effectively reach your global audiences.

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