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Transforming Medical Affairs Practices with AI and Automation for Scalable Impact

Life sciences organizations are turning to AI to enhance operational efficiency, and one of the hottest areas of interest is the integration of AI and automation for medical affairs workflows. Beyond process optimization, automation has been accelerating omnichannel strategies by enabling and improving precise, personalized, and scaled communications with patients and healthcare professionals. As a key strategic partner to many parts of an organization, medical affairs...

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The Ultimate Guide to AI in Pharmacovigilance and Safety Reporting

Pharmaceutical companies face stringent compliance requirements and tight deadlines for reporting safety cases throughout clinical research and development. To protect patient safety and avoid penalties from regulatory authorities, pharmacovigilance teams must submit in-language reports on time. AI technology offers transformative solutions to these challenges and opens the door for increased efficiencies throughout event observation, detection, and monitoring. This guide...

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The Paper Chase - Clinical Outcome Assessments in the Digital Age

Patients are, at last, gaining a voice in healthcare. Stakeholders have come to recognize that patients have valuable information to share about their experiences with diseases and medications that should influence policy and treatment decisions. The U.S. Food & Drug Administration (FDA), for example, has launched an initiative, “The Voice of the Patient,” to gather patient perspectives across specific disease areas. Information reported by clinical trial participants...

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The Total Economic Impact of TransPerfect GlobalLink for Life Sciences

TransPerfect commissioned Forrester Consulting to conduct a Total Economic Impact™ (TEI) study and examine the return on investment (ROI) enterprises may realize by deploying GlobalLink. The objective of the framework is to identify the cost, benefit, flexibility, and risk factors that affect the investment decision. Forrester took a multistep approach to evaluate the impact that GlobalLink can have on an organization. The purpose of this study is to provide readers with a...

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Wearables for eCOA: Practical Considerations for Improving Patient Data Capture

This electronic clinical outcome assessment (eCOA) webinar will explore the latest advancements in wearable technology and their potential to improve patient data collection in clinical studies. While there may still be ongoing discussions around deployment and standardization, it is clear that newer technologies such as accelerometers and video have the ability to passively or proactively gather more patient data. These wearable devices offer significant advantages in terms...

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Transitioning Clinical Trials Under the EU CTR

The transition from Clinical Trial Directive to Clinical Trial Regulation in Europe adds new requirements and complexities to the clinical development landscape. The required transition of all trials concluding January 1st, 2025 brings about several considerations to ensure compliance. In this webinar featuring TransPerfect Life Sciences Executive Director Pierre-Frederic Omnes, we explore topics surrounding trial transitions, and answer common questions including: • Which...

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Unlocking the Power of AI and Machine Learning in Life Sciences

Life sciences companies are putting artificial intelligence (AI) and machine learning (ML) into practice, realizing its potential to revolutionize adverse event detection, diagnostics, and more. For AI and ML to be truly effective, you need to give context to your data, teaching the systems to analyze information and improve processes. This is done through data annotation. Discover immediate steps to leverage the power of AI/ML and easy solutions to get you started in this...

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Xtalks Webinar: Artificial Intelligence and Structured Data: Driving Process Efficiency for Medical Device Manufacturers

Since the advent of artificial intelligence (AI), medical device manufacturers have been early adopters for product enhancements. Now, manufacturers are evaluating their regulated content and other production processes for suitable applications of AI and automation technology. Moreover, while AI offers unprecedented opportunities for increased efficiency, accuracy and quality, it also requires a strong foundation of structured data and an awareness of global regulatory...

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Life Sciences Learning Trends - Office Hours Q&A

Join the TransPerfect Learning team for an interactive virtual C3 Study Session, focused on the latest commercial learning trends transforming the life sciences industry. Whether you attended LTEN 2025 or are simply passionate about advancing learning & development in your life sciences organizations, this session is designed for you! Gain firsthand insights from Tim Robinson (Head of Learning Experience), Sarah Minkoff Stevens (Senior Learning Manager), and Gracie...

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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 who can...

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Process AI in Medical Device: What Works and What’s Next

The webinar will also explore the use of Process AI across life sciences operations. Instead of treating each process, such as post-market surveillance, complaint handling, systematic literature review and regulatory content authoring, like separate AI projects, this session will show how the same core tasks (like classification, extraction, summarization and generation) can be mixed and matched. With these building blocks in place, attendees will be able to create reviewer...

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RAPS Conference Takeaways

The Quick Conference Catch Up is a device industry reporting service from TransPerfect Medical Device. Based on live attendance at premier regulatory and strategy conferences, each Catch Up uses a conversational format to recap and highlight key conference takeaways. In these short video summaries, you will find insights on headline device industry issues, while saving the time and expense of in-person attendance!...

Pharmacovigilance and Safety Solutions

Observe, detect, and monitor the effects of your pharmaceutical products across locations and languages with translation and call services. Ensure drug safety across your entire portfolio....

Medical Writing and Content Solutions

Simplify content creation for a range of audiences and ensure timely, quality, and compliant scientific, technical, medical, regulatory, and commercial communications....