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E-Learning in Pharma: Creating & Managing Global Training Programs

From compliance and standard operating procedures (SOPs), to product info and sales techniques, e-learning ensures global teams have access to top-notch, consistent, and on-demand training. This guide explores key considerations for effective and engaging global e-learning content, what to consider when choosing an e-learning partner, and how centralizing training management can help pharma companies launch content more quickly while saving up to 40%....

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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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LifeSci Talks COA Series | From Interview to Endpoint: Understanding the Importance of Patient Listening to Build Better Outcomes

In this episode of TransPerfect LifeSci Talks, Mark Wade, Global Practice Leader at TransPerfect Life Sciences sits down with John Reites, Co-Founder and CEO of THREAD research to discuss the importance of patient listening to build better clinical trial endpoints. They delve into the differences between enterprise and standalone solutions, challenges with standardization, and the influence of evolving technologies in the eCOA industry. ...

Translation Strategies for Safe, Cost-Efficient Clinical Trial Content

Pharmaceutical, biotechnology, and medical device organizations cannot afford translation errors. A single mistranslated word on a product label, medical instruction, or clinical document can cost millions, delay approvals, and even put patient lives at risk. This guide outlines the key translation risks, strategies, and solutions that life sciences leaders need to know for flawless content localization. By developing a comprehensive translation strategy for each of your...

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Scaling Global Campaigns with AI and Human Expertise: Lessons from Sanofi

Navigating the complexities of global healthcare campaigns requires a well-balanced mix of technology and human touch. In this webinar, TransPerfect welcomes back Krista Goedel, Clinical Digital Content Lead along with colleague Lyly Fong, Global Corporate Website Manager at Sanofi, who will discuss how AI-driven content creation, combined with human expertise and oversight, is transforming global campaigns. Gain insights into how Sanofi uses GlobalLink to maintain brand...

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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...

Sign Up for Free Office Hours

Address challenges in clinical development, regulatory compliance, and patient engagement with an expert. TransPerfect Life Sciences offers a unique opportunity for free consulting through office hours with our subject matter experts. Explore some of your most pressing questions, without the cost or sales pitch. ...

XCompare - COA Migration

Reduce eCOA migration errors with XCompare technology that automates your development and translation workflows....

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LifeSci Talks | Effective Rater Training: A Critical but Overlooked Part of COA Administration

In this episode of LifeSci Talks, TransPerfect Life Sciences’ Global Practice Leader Mark Wade sits down with Kelly Dumais PhD, Director of eCOA Science at Clario to discuss the significance rater training plays in standardizing the administration and scoring of clinical scales. Aiming to reduce bias and enhance data quality, you’ll hear about potential strategies for better engaging patients and how comprehensive proactive training can reduce patient and site burden. Listen...

Training & Development

Ensure all employees are trained on protocol, regulatory, and SOP compliance to improve patient safety and GDPR compliance. ...

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Harnessing AI in Pharmacovigilance: Insights from World Drug Safety Amsterdam 2024

Pharmacovigilance professionals face an escalating challenge: data overload. From AI-powered transcription and case triage to automated literature translation, insights from the World Drug Safety Congress 2024 showcased practical solutions for streamlining workflows and reducing costs. Download the PowerPoint from Christine Buggle's presentation on this topic....