Resource

Driving Strategic Change: General Counsel in Pharma

TransPerfect Legal Solutions hosted a panel of GCs and legal experts from prominent pharmaceutical companies to discuss their evolving roles and the practical ways legal departments are driving innovation as it relates to people, risk, and data in the pharma industry. PANELISTS: Zafar Qadir – General Counsel, Bicycle Therapeutics Alexandra Pygall – Partner, Head of Life Sciences, Stephenson Harwood Keir LoIacano – Counsel and Vice President of Corporate Development,...

Resource

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%....

Resource

EU CTR: An Introduction to European Clinical Trial Transparency

Are you looking to stay ahead of the curve in the ever-evolving landscape of European clinical trials? We are thrilled to announce the availability of our newest on-demand webinar, in which we dive deep into the recent changes to the European Clinical Trial Regulation (EU CTR) and how they impact the world of clinical research. Access this webinar and gain invaluable insights on: 1) Overview of the new EU CTR: Understand the latest regulations governing clinical...

Resource

Generative AI in Life Sciences Industry: Ethics, Applications, and Transformations

Discover the role of generative artificial intelligence (GenAI) in life sciences, including what is merely a trend vs. what is truly transformative. The speakers will explore pragmatic applications, ethical considerations and the potential future role of generative AI in life sciences, research and development (R&D) and product development. The discussion will provide valuable insights into the ongoing AI revolution within the life sciences sector, including practical...

Resource

GenAI Strategies for Life Sciences: Creating Content that Performs, Complies, and Resonates

Everyone’s talking about GenAI, but what does it really mean for pharma communications and promotional materials? Join our life sciences and AI experts in a follow up session from Search, Reinvented Evolving SEO in the Era of LLMs and GenAI, where we’ll take a closer look into how large language models are changing how we create and find content. This session will cover what effective SEO looks like today and how to create content that not only ranks but resonates,...

Resource

Faster Submissions, Smarter Workflows: Lessons from Sanofi's AI-Powered Translation Strategy

In this session, learn how Sanofi has transformed its translation processes using centralized management by expert project managers, automated workflows, and integration of TransPerfect’s GlobalLink platform with Veeva eTMF. You’ll gain insights into Sanofi’s pragmatic, phased approach, including leveraging automation and AI-powered workflows. The result is a dynamic digital ecosystem that captures feedback, drives continuous improvement, and achieves over 30% savings in time...

Resource

Foundations of Clinical Outcome Assessment Localization

Accurate and culturally appropriate translation of clinical outcome assessments (COAs), including patient-reported outcome measures, is essential to ensuring reliable data in multinational trials. Foundations of Clinical Outcome Assessment Localization will provide a practical overview of why linguistic validation goes beyond standard translation and how it safeguards both data integrity and patient understanding. The session will cover current regulatory guidance, the steps...

Resource

Fast, Compliant, Centralized Translation in Action: Lessons from AbbVie & Immunovant

Due to high interest following our GlobalLink NEXT panel, we’re welcoming back Stacey Higgins, Associate Director, COA & Digital Implementation Team of AbbVie alongside Tihirah Harris, Sr Manager, Clinical Business Operations of Immunovant to share how and why they moved to a centralized, tech-enabled translation model—enabling faster trial timelines, cost control, and regulator-ready content. We'll also cover what’s ahead on their centralization roadmap, including...

Resource

GL - Machine Translation Success in Life Sciences

From clinical trial documentation to patient communications and to post-market materials, machine translation (MT) enables fast, and cost efficient communication in various languages worldwide. This guide shares case studies of impactful AI and MT implementations for leading pharmaceutical, biotech, and medical device companies. Download now to see how your life sciences peers reduce translation cycle times, increase speed of global communications by 75%, and more. ...

Resource

Improving Learning Outcomes in Life Sciences Through Data-Driven Benchmarking

In life sciences, strong training programs are essential, but knowing whether they’re actually effective can be a difficult endeavor. In this session, Amanda Hernandez, Director of Sales Training & Effectiveness and Barrett Gaylord, Sales Training Lead of Telix Pharmaceuticals alongside Jessica Peyser, Senior Director at TransPerfect Life Sciences, discuss practical ways to benchmark training performance to help teams see where their programs are meeting performance...

Resource

Integrating AI to Scale & Accelerate Workflows and Improve Pharma Product Launches

Bringing a new medical product to market has always been a challenge, though advances in recent tools have promised a new age of streamlined processes and accelerated time to launch. However, most pharma commercial AI pilots never make it past proof of concept due to siloed workflows, data fragmentation, regulatory and IT bottlenecks, and quality risks. Join us for a webinar with TransPerfect’s commercial and AI experts, who will walk through practical workflows and...

Resource

Human & Animal Blood Cell Image Annotation Spotlight

An award-winning healthcare AI company specializing in using the best in human and computational intelligence approached DataForce to build an external team with a background in biology to review and annotate thousands of microscopic images of blood smear samples. With 30,000 images across six species, our client was looking to deliver precise and individualized healthcare while also ridding the world of preventable diseases through rapid at-home testing for immune health. To...

Resource

How to Maximise Value and Avoid Failure During Life Sciences Dealmaking

Please complete the form below to access the on-demand recording of our webinar. A fantastic expert panel of life sciences dealmaking veterans from AstraZeneca and Merck, with 100 years' collective experience, share their insights on key dealmaking strategies, best practices, and common pitfalls to avoid in order to maximise value and mitigate risk in life sciences dealmaking, and also answer audience questions. Topics discussed include: - The importance of...

Resource

Global by Design: Localizing UI/UX for Health Mobile Apps

In today’s global digital health landscape, localization goes far beyond translation. In health mobile applications, it means tailoring the user experience to cultural, linguistic, and even regulatory nuances across different regions. This discussion explores how localization in UI/UX design can significantly improve accessibility, trust, and engagement with health apps around the world....

Resource

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....

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

Lessons Learned from SCMS Deployments in Global Medical Device Documentation

Transitioning to modular content using a Structured Content Management System (SCMS) has the potential to transform medical device documentation by streamlining authoring and automating content updates and publishing. For a truly successful implementation, however, early planning and strategic alignment are essential. In this webinar, we welcome back industry experts from Bayer, Medtronic, and Carestream for an insightful discussion around how structured data, automation, and...

Resource

Intelligent Automation for MDR & IVDR Content: Summary of Safety & Clinical Performance (SSCP), Summary of Performance (SSP), and Selected Labeling

Content requirements under the EU’s MDR and IVDR, including the translation of labeling, marketing, SSCPs, SSPs, and clinical communications, are set to dramatically increase. Currently, most device manufacturers use manual processes and document-based applications like Microsoft Word and InDesign to manage their content. However, manual processes and document-based approaches require additional headcount to handle increased volumes and faster turnarounds. Download our paper...

Resource

Integrating eCOAs and Digital Health Technologies for Patient-Centric Trials

The foundation of patient-first design is technology that connects seamlessly to support and meet patients where they are. In this session, leaders from Pfizer, THREAD, Datacubed, Obvio Health, and Merative will discuss how integrated digital ecosystems are breaking down platform and industry silos, enhancing engagement, improving access, and scaling across therapeutic areas. Learn how pharma and tech companies are expanding digital endpoints and paving the way for the next...

Resource

Translation and Cultural Adaptation of Clinical Outcome Assessments (COAs): Is Machine Translation a Viable Option?

As technology continues to advance and the need to expedite drug development increases, the applications of Machine Translation (MT) and Artificial Intelligence (AI) in the translation process should be further explored. The capabilities of iterative learning and feedback can serve as a tool for translation, but the limitations should be considered. This poster will compare human translation (HT) and machine translation (MT) in the back translation step for Clinical Outcome...