Thought Leadership
Digital Transformation Fireside Chat
In this fireside chat, Christine Buggle-Spearing and Dr. Gigi Shafai, Pharm.D., from TransPerfect Life Sciences, share practical strategies for modernizing medical affairs processes. The discussion covers how to design a digital-first strategy that creates value for both patients...
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...
LifeSci Talks COA Series | Silver Bullet or Useful Repositories: The Reality of Clinical Trial Libraries
In this episode of LifeSci Talks, Mark Wade, Global Practice Leader at TransPerfect Life Sciences, is joined by Jonathan Norman, Director of Translation and Localization at YPrime, for an in-depth discussion on the realities of eCOA libraries. Together, they explore why ...
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...
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...
C3 Summit - 2025 | San Francisco
AC Hotel San Francisco Airport/Oyster Point 1333 Veterans Blvd, South San Francisco, CA 94080...
Structured Content Simplified: A Practical Guide for Veeva, XML, and Beyond
Life sciences organizations are facing increasing pressure to deliver accurate, compliant content across multiple channels and global markets faster than ever. To keep pace, many are turning to Structured or Component Content Management Systems (SCMS/CCMS), which allow teams to...
AI-Powered Literature Monitoring for Medical Affairs & Medical Information Teams
Automate literature monitoring with AI. Boost accuracy, speed, and security for medical affairs teams. Streamline workflows and enhance global insights today....
Improving Learning Outcomes in Life Sciences Through Data-Driven Benchmarking
Avoid localization mistakes in 2025. Improve website localization, boost local SEO best practices, and reach global audiences. Learn more today. ...
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...
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...
How Patients Discover Clinical Trial Websites: The Role of Localization in Search and Trust
Could localization be the key to improving patient recruitment in clinical trials? ...
LifeSci Talks COA Series | Modernizing eCOA: Emulators, Backups, and the Future of Reporting
In this tech-forward episode of LifeSci Talks, Mark Wade, Global Practice Leader at TransPerfect Life Sciences, welcomes Indira Jain-Figueroa, Product Director at Evinova, for a deep dive into the ever-evolving landscape of eCOA development. Covering everything from cross...
Rewriting the Rules of Informed Consent Development with AI
ICF development is resource intensive and costly. Learn how forward-thinking teams are streamlining the process with powerful AI tools....
Could Data Standardizations be the Silver Bullet for Faster Electronic Clinical Outcome Assessment (eCOA) Deployment?
Choosing an electronic clinical outcome assessment (eCOA) provider is a complex process that involves a variety of different aspects including experience, scientific support and knowledge, integration capabilities, scalability, study-specific requirements, and so much more. ...
Accelerating Pharma Labeling with Intelligent, Compliant Content
Juggling multilingual labels across varying regions and products? Managing the updates and complying with local health authorities' requirements can be a challenge for global pharmaceutical companies, who are facing increasing pressure to streamline labelling processes and...
Engaging Patient Communities: A Pathway to Clinical Trial Success
In this webinar, expert speakers from MTS Sickle Cell Foundation, Inc, Rare Disease Diversity Coalition, Black Women’s Health Imperative, and Clinical Research Associates, Inc. will focus on the critical role of patient communities in advancing clinical trials. They will...
Health Canada's Transition to XML: What Regulatory Teams Need to Know
Health Canada’s shift to XML Product Monographs starts July 2025. Learn what regulatory and compliance teams need to do now to stay aligned and submission-ready....
LifeSci Talks COA Series | Balancing Innovation and Integrity: AI’s Place in Patient-Focused Research
Artificial intelligence is redefining what’s possible across the clinical development lifecycle, but with rapid innovation comes the need for thoughtful oversight. In this episode of LifeSci Talks, Mark Wade, Global Practice Leader at TransPerfect Life Sciences, sits down with...
Web Localization Playbook for Life Sciences
The life sciences industry relies on websites to connect with patients, sites, and global audiences. Whether you're launching a patient recruitment campaign or managing an international healthcare marketing initiative, localization ensures your message is not just understood...
6 Ways to Take Your Machine Translation Strategy to the Next Level
Future-proof your MT strategy for clinical and regulatory content with this guide....
Rewriting the Rules of Informed Consent Development with AI
Regardless of the market a clinical trial is being conducted in, getting locally approved informed consent forms (ICFs) consume as much as 12% of a clinical trial budget before it even begins. Each ICF must be clear and delicately balance local regulations and patient...
Multilingual IMP Labeling Quick Guide
Meet global regulatory expectations the first time with these efficient, cost-effective, and compliant product labeling solutions and considerations....
OpTImize London
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