Deliver An Omnichannel Experience With Medical Affairs Global Content Strategies

Reach your audience faster in a conceptually equivalent, culturally appropriate and compliant way.

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Customer-centric focus to effectively engage and educate key stakeholders, no matter the language

Increasingly specialty medicine requires increasingly specialized education. The methods to deliver digital content are multiplying. The way physicians consume medical content is evolving. All of the above create complexity for medical affairs teams trying to deliver high-quality, engaging content.

With 30+ years of experience, TransPerfect Life Sciences helps MedAffairs teams adapt their communications to effectively reach patients, sponsors, CROs, HCPs, and the general public in compliance with local regulations.

patient engagement in clinical R&D

Evolve Your Medical Affairs Operations From a Regional to a Global Integrated Model

With our expert localization and content adaption service for medical affairs teams, we have helped them see a reduction in content development costs by over 25%.

Why Choose TransPerfect Life Sciences for your Medical Affairs Content Creation and Adaption?

  • >25% Reduction in Content Development Costs
  • Future-Proof Scalability with Technology Driven Workflows and Integrations
  • Flexible and Customizable
  • Fully Integrated Model With Knowledge Management Systems and Processes

Even simple changes to the language of medical affairs content can significantly impact the effectiveness of global messaging.

We make sure your communications relay exactly what you mean, regardless of who you’re speaking to. 

News and Press Releases

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

The Ultimate Clinical Trial Translations 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

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 ...

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 ...

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 ...

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,...

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...

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...

Interested in learning how we can help your Medical Affairs content strategies?