Clinical, regulatory, and commercial teams all rely on the same content, yet often work in siloes. This white paper examines the real cost of disconnected content strategies and why localization should be treated as a strategic input, not a final step. Discover how global-ready content reduces duplication, improves consistency, and enables faster global deployment without sacrificing compliance or quality....
Medical communications teams are under mounting pressure to review more content than ever before without adding headcount or increasing risk. This white paper outlines five pillars for rethinking MLR workflows, from modular content and tiered reviews to automation and governance. Get a realistic roadmap to alleviate team burnout, scale reviews, remove bottlenecks, and stay compliant....
Multilingual trial SEO is critical to ensure that patients and HCPs can actually find and act on your trial content in their language. This checklist walks clinical trial teams through five essentials:… ...
In this episode of LifeSci Talks, Mark Wade, Global Practice Leader & COA SME at TransPerfect Life Sciences, is joined by Katja Rudell, VP of Patient-Centered Outcomes at Kielo Research, to take a behind-the-scenes look at the reality of patient-centered instrument development. They discuss diaries and quality of life tools, rare disease challenges, and proxy reporting, as well as the tradeoffs that can often occur in balancing regulatory rigor, patient burden, and...
Deploy evidence-based patient engagement tools to increase compliance and elevate product readiness. Meet the ever-growing needs of patient-centric and inclusive solutions. ...
Streamline global development and commercialization of products through content solutions and specialized services developed by industry experts for sponsors and CROs....
A Top 10 pharma needed to accelerate clinical and regulatory translations without increasing compliance risk or slowing submissions. This case study shows how they kept content inside Veeva Vault with an automated integration and a hybrid model (AI + validated translation memory + expert review), delivering millions in savings and getting hundreds of working days back while improving quality oversight across…...
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: it's trusted, actionable, and compliant. In this downloadable playbook, learn more about effective web localization and the technologies will power it in 2025 and beyond. ...
Clinical trial websites are recruitment engines. Every update must stay accurate, compliant, and consistent across languages. Yet many teams still manage localization with file handoffs, dev tickets, and manual copy/paste that can’t scale. This playbook covers… ...
Deploy evidence-based patient engagement tools to increase compliance and elevate product readiness. Meet the ever-growing needs of patient-centric and inclusive solutions. ...
Deploy evidence-based patient engagement tools to increase compliance and elevate product readiness. Meet the ever-growing needs of patient-centric and inclusive solutions. ...
Language barriers are a measurable enrollment risk, and one that compounds fast. The gap between a localized and non-localized clinical trial website is wider than most teams expect, touching everything from regulatory compliance to participant drop-off. This infographic breaks down the financial, operational, and compliance case for getting it right, what happens when teams skip it, and…...
Simplify content creation for a range of audiences and ensure timely, quality, and compliant scientific, technical, medical, regulatory, and commercial communications....
Access end-to-end consultation, from licensing to electronic clinical outcome assessment (eCOA) migration, and improve the patient and healthcare provider experience with all types of COAs. ...
In this episode of LifeSci Talks, Mark Wade, Global Practice Leader at TransPerfect Life Sciences, sits down with Dr. Kate Williams, Director of Patient-Centred Outcomes Research at Acaster Lloyd, to explore the nuances of gathering and applying qualitative data in rare disease research. From intaking both the patient and caregiver experience using a narrative approach, to qualitatively describing the experience of living in different disease states, the two focus on the...
The rare disease space presents numerous challenges for clinical research and patient data capture. These challenges are only heightened for younger patient populations, where outcome measures and dosages need to be considered appropriately. Join Dr. Elin Haf Davies, Founder & CEO of Aparito, in conversation with Mark Wade, Global Practice Leader at TransPerfect Life Sciences, as they discuss: The disparity in data capture for pediatric populations. Considerations for...
Gain insights into your product’s success through monitoring patient and customer feedback, conversations around your target keywords, competitors, industry topics, brand mentions, and more on global social media networks. ...
We offer a full suite of clinical trial disclosure services led by transparency subject matter experts to meet requirements and publish clinical trial results with speed and quality in any language. ...
Delivering seamless customer-centric communications to key stakeholders around the world through effective omnichannel strategies....
Automate your redaction process and protect sensitive information with TransPerfect’s AI technology and team of professional redaction specialists....
