Life Sciences
at Vistatec
Translation and localization for essential medical services.
Life Sciences
at Vistatec
Translation and localization for essential medical services.
The Vistatec dedicated Life Sciences Division understands the importance of specialized workflows and expertise to deliver solutions for leading organizations worldwide.
Our clients benefit from accurate and high-quality solutions, with industry-leading expertise demonstrated across a portfolio that includes medical devices, health care software, clinical trials, biotechnology, mental health, pharmaceuticals, and pure and applied science.
We provide multilingual support at every stage of the product life cycle.
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Life Sciences Podcasts
Catch up on the latest episodes of our Life Sciences — In Focus Podcast. View the videos below, or visit the show page on Spotify, YouTube, or Apple Podcasts.
Ep 16 - Eloise Moffet
“Sometimes, going back to basics is the boldest move you can make.” That sentiment perfectly captures the perspective shared by Eloise Moffett, Vice President of Commercial at Innovative Trials, in the latest episode of the Life Sciences – In Focus podcast.
From cultural nuance in global patient engagement to bold marketing campaigns that make a meaningful impact, Eloise brings passion, creativity, and authenticity to her role and the wider clinical trials landscape.
Watch Previous Episodes:
Life Sciences Events
Life Sciences — In Focus Panel Discussions
Ep 7: Laboratory Developed Tests: What Now, Where Next?
This Life Sciences – In Focus Panel brought together leading regulatory experts to discuss a hot topic in the diagnostics industry: Laboratory Developed Tests (LDTs) and their tumultuous regulatory journey. Hosted by Karen Tkaczyk, Director of Sales at Vistatec Life Sciences, the panel featured Cortez McBerry (Regulatory Consulting Director at NDA Partners), Sean McCarthy (Senior Regulatory Manager at Enhanced Compliance, Inc.), and Tristin Wolff Cope (Director of Regulatory Compliance at Biodesix). Their insights not only unraveled the complexities of LDT oversight but also emphasized the pressing need to bridge gaps in regulatory frameworks.
Ep 6: Amplifying Patient Voices in Clinical Research: Strategies for Engaging Non-English Speakers
Clinical trials serve as the backbone of medical innovation, yet a significant portion of the global population remains underrepresented due to language barriers. In this episode, moderator Karen Tkaczyk led a compelling discussion on strategies for engaging non-English speakers in clinical research. Featuring Julie Blasingim (CEO, Univo IRB), Harsha Rajasimha (CEO, Jeeva Clinical Trials), and Lya Rebelo (Commercial Enablement Manager, Citeline), the conversation tackled regulatory challenges, ethical considerations, and the role of technology in fostering inclusivity.
Ep 5: Breaking Barriers: Enhancing Diversity and Inclusion in Clinical Research
Clinical research holds the key to groundbreaking treatments and improved health outcomes. But for far too long, it has struggled to represent the people it aims to serve—particularly underserved communities. A recent Life Sciences – In Focus panel discussion titled “Breaking Barriers: Enhancing Diversity and Inclusion in Clinical Research” shed light on these systemic issues while offering innovative, practical solutions to create more equitable and inclusive trials.
Ep 4: FDA Diversity Action Plans: Deciphering the Guidance and its Consequences
The US Food and Drug Administration has released long-awaited updated guidance on Diversity Action Plans. This guidance is stronger and very specific in places. In this panel discussion, Vistatec invites industry-leading experts Aman Khera, Joan A. Chambers, and Lya Rebelo to explore how both large and small sponsors are responding to these changes. Through real-world examples, they discuss the implications of these plans on site burden, patient experience, and how clinical operations and regulatory affairs teams are applying this US-focused guidance in global trials. Click the video to watch the recording of this essential conversation.
Ep 3: Navigating the Regulatory Landscape - Latin America Edition
Through case studies and real-world examples, learn from success stories and lessons gained from navigating the complex regulatory environment in Latin America. Vistatec invited industry-leading experts to share the latest regulatory updates and trends and understand their implications for clinical research and development. Click the video to watch the recording of the panel discussion.
Ep 2: Real-World Evidence: Global Regulatory Landscape and Innovation
Real-world evidence (RWE) has been a hot topic in recent years, not only in the research and life sciences industry but also in public health. Given the challenges surrounding its ethical use and regulation, the increasing importance of AI and the sheer volume of data available, the discussion is sure to continue. Vistatec invited industry-leading experts to share their insights, thoughts, and predictions on the role of RWE going forward. Click the video to watch the recording of the panel discussion, or read the key learnings here.
Ep 1: Leveraging Data and Trends for 2024
In the first installment of Vistatec’s Life Sciences – In Focus series, Amanda Murphy, Senior Director of Data Intelligence and Solutions at GlobalData, presented the biopharmaceutical industry’s outlook for 2024. The event yielded valuable insights into the trends and themes predicted for the upcoming year, focusing on the clinical trials landscape, including decentralized clinical trials and diversity. Click the video to watch the recording, or read the key learnings from the event here.
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Life Sciences Experts
Kara Bolt
Director
Life Sciences Division
Karen Tkaczyk, PhD
Director of Sales
Life Sciences Division
Maria Mateos
Strategic Account Director
Life Sciences Division
Erin Nye, Illumina
Think Global Forum
Richard Korn, Edward Life Sciences
Sean Kinsell, Medidata