Helping Life Sciences Organizations Reach More Patients

International Marketing Solutions for the Life Sciences Industry

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Targeted Patient Campaigns for Anywhere in the World, in Any Language

Roughly 80% of clinical trials fail to meet enrollment timelines.

Approximately one-third (30%) of Phase III study terminations are due to enrollment difficulties.

As these statistics make abundantly clear, better patient recruitment processes can drastically improve clinical trial success.

Create Strategic Global Patient Recruitment Campaigns

We can help with our extensive market research, global expertise, and local digital marketing experts

  • Market Insights – Mapping the Patient Journey
  • Cultural Consulting – Adapting Content for Intended Audiences
  • Regulatory Consulting – Advising on Local Regulations (e.g., Promotional Liability in the EU)
  • Medical Writing & Content Development
  • Digital Strategy
  • Translation and Media
  • Technology to Streamline Approval Process
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Be Where Your Patients Are—Effective Digital Strategies For Patient Recruitment

Did you know that 15–20% of studies do not launch due to unsuccessful patient enrollment? In the past, recruiting the RIGHT patient population has been complex, expensive, and challenging, especially when it comes to rare diseases or niche requirements. 

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Benefits of TransPerfect's Digital Patient Engagement Solutions

Patient recruitment consumes 27% of the cost of development–that is $5.9 billion annually around the world.

Timelines

Shrink Timelines for Creating and Launching Campaigns

Save Money

Save Money on Campaign Planning and Execution

Marketing

Retain More Patients with Improved Targeting and Patient Education

Regulatory

Maintain Protocol Adherence and Reduce Compliance Risks

Streamline Patient Recruitment Strategies

A diverse and inclusive patient recruitment strategy is key to ensuring a successful clinical trial. TransPerfect Life Sciences supports pharmaceutical companies in reaching patients, meeting enrollment numbers, and meeting diversity and inclusion goals. With extensive market research and global expertise, our local digital marketing experts develop strategic recruitment marketing plans and messaging that engage patients across all channels.

News and Thought Leadership

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

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...

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