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    Featured

    C3 Summit London 2025

    event 8 Northumberland Ave
    London WC2N 5BY, UK | May 8, 2025

    Conversations on Clinical Content, C3 Summit is part of a series of events hosted by TransPerfect Life Sciences featuring sessions with expert panels discussing present challenges, strategies, and innovations, as well as insights into future advancements, from R&D to...

    Learn more ›
    • COA/eCOALifeSci Talks COA Series | Making the Most of Smaller Population Samples: Qualitative Insights in Rare Disease
    • AI/MLAI in Clinical Outcome Assessment (COA): Challenges and Opportunities
    • GlobalLinkThe Total Economic Impact of TransPerfect GlobalLink for Life Sciences
    • Medical DeviceRAPS Conference Takeaways
    • Med WritingAI and MT for Medical Information Office Hours -4/30/2025
    • PV & SafetyAI and MT for PV and Safety Office Hours - 4/23/25
    See all Resources ›

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    Innovation Spotlight

    Industry Leading AI-Powered Innovation

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    • eclinical Trial Interactive eClinical Platform
    • R&D AI Portal
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Blog

The Importance of Over-the-Phone Interpretation for Emergency Services

Blog

Leveraging the Patent Priority Date: A Life Sciences Focus

Blog

How CCMS Helps Healthcare Companies Prepare and Translate Medicare Compliance Content

Blog

3 Translation Methodologies for Life Sciences Documentation

Blog

How TMF Study Owners Can Provide Better TMF Management

Blog

How to Choose and Implement a CTMS

Blog

How Life Sciences Companies Can Detect Adverse Events on Social Media

Blog

The Summary of Safety and Clinical Performance (SSCP) for Healthcare Professionals and Patients

Blog

Driving Fundamentals: Ensuring an Efficient Clinical Research Process

Blog

Practical Applications of Machine Learning for Clinical Trials

Blog

ICH E6(R3): Understanding the Updated Good Clinical Practice Guidelines (GCP) and Their Future Impact

Blog

4 Immediate Applications for AI Translation in Pharma

Blog

Navigating the Bias Challenge: Medical Data for Ethical AI in Life Sciences

Blog

Localizing Platforms for Digital Health: The Importance of Post-Localization Context Review

Blog

How to Approach the Protection of Personal Data and Commercially Confidential Information of EU Clinical Trial Applications: Practical Considerations

Blog

Clinical Outcomes Assessments (COAs) in Clinical Trials: Copyright and Licensing

Blog

The Role of Qualitative Interviews in Ensuring a Patient-Centered Approach to Clinical Trials

Resource

How to Increase Your Likelihood of Scientific Publication

Writing a scientific manuscript involves considerable planning and organization to boost your chances of publication in a peer-reviewed journal. Here, we show you how to develop a thorough plan to present research logically and how to avoid the common pitfalls of authorship, so you can overcome the chances of rejection for publication....

Resource

A Checklist for eCOA Solution Deployment: Best Practices and Considerations

Selecting and deploying a new eCOA solution involves many important factors - from determining the capabilities of the Language Service Provider (LSP) to identifying the technology used for each COA migration - and it’s impossible not to worry about missing a key detail in the process. Download our whitepaper to learn about the eCOA landscape today, and access a checklist that walks through each of the essential factors to consider so you can be confident your eCOA...

Resource

Top 10 Biotechnology Company Captures and Disseminates Insights from a Key Advisory Board Meeting

The company enlisted the support of TransPerfect to provide a medical writer with expertise in the genetic disease to transcribe the meeting in full and produce an executive summary detailing the main takeaways and discussions....

Resource

Clinical Data Services Company Launches its Statistical Webinar Series

“Another great seminar in a long line of excellence. I can only say, keep it up!”...

Resource

Leading Japanese Pharma Company Authors High-Quality Regulatory Documentation

TransPerfect provided medical writing support with subject matter expertise and key regulatory experience to produce high-quality ICFs and a protocol....

Resource

Global Pharma Saves $1.1M with Regulatory Translation Solution

AI-powered workflows to help reduce costs and timelines while being scalable to the large volume of content required....

Resource

ISPOR Europe 2020 Virtual Poster - Usability Testing for eCOAs

In order to ensure a fluid experience for a patient, usability testing is a critical data point to consider. Addressing both a patient’s needs and access to a digital platform is key to data collection. TransPerfect, along with our partners from Parexel, Clinical Ink, and Health Psychology Research, recently published a poster at the Virtual ISPOR Europe 2020 conference that reviews the impact of moving from in-person to electronic data collection....

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