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. 

Get in Touch
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
Learn More

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
Learn More

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
Learn More

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 Ultimate Clinical Trial Translations Checklist

Checklist

Clinical product development is an elaborate endeavor executed through a complex web of processes that are in large part accomplished through various document and communication work streams. These work streams can represent a significant source of cost, risk, and time. When a study operates across cultures, countries, and continents, these pain points of cost, risk, and time are compounded by the addition of translation and localization requirements. Study teams ...

The Ultimate Clinical Trial Translations Checklist
Webinar

CCMS: A Good Fit for Pharmaceutical and Clinical Research Organizations?

Kaarin Gordon discusses the choices and challenges for efficient content reuse facing Pharmaceutical and Clinical Research Organizations. What they want is a set of tools and platforms for easy content reuse, automatic propagation of changes from a single source, and content ...
White Paper

Omnichannel Marketing for the Pharmaceutical Industry

With rapid globalization and expanded marketing efforts, pharmaceutical organizations are discovering that pivoting from multichannel marketing to omnichannel marketing is key to revolutionizing patient engagement. Through tailored experiences across relevant channels, your teams ...
Webinar

LifeSci Talks COA Series | The Future of Capturing Patient Data in Clinical Trials: DCTs, Site Staff Burden, and Regulation Considerations with Paul O'Donohoe

Mark Wade interviews Paul O'Donohoe, Senior Director of Product for eCOA and COA at Medidata. They delve into the challenges and opportunities of adopting decentralized clinical trials (DCTs) and explore topics such as mixed modalities for data capture, patient burden, site ...
Blog

Walking the Tightrope: Navigating Patient Centricity and Burden in Modern Clinical Trials

Over the past few decades, clinical trials have witnessed remarkable developments - but they are not without challenges. Dropout rates of up to 20% indicate that patient burden and engagement remain key areas of concern. In response to this, sponsors, healthcare providers,...
Blog

Health Canada's XML Mandate: Pioneering the Future of Pharmaceutical Content

In 2019, Health Canada initiated a significant process to transition all product monograph templates into a more advanced and structured XML format. This move by the regulatory authority has raised several questions for Canadian pharmaceutical organizations' regulatory and...
Blog

Leveraging Technology and Bridging Gaps for Enhanced Clinical Data Management

Introduction: In the field of clinical research, a robust data management process is essential for driving success. Efficiently handling vast amounts of data, ensuring accuracy and consistency, and extracting meaningful insights are vital, particularly in the case of global...

Effectively reach your global audiences.

Get in Touch ›