Thought Leadership
Maximizing Learning on a Budget: 3 Cost-Effective Strategies for Clinical Education and L&D in Medical Device Companies
Are you struggling to provide high-quality training to your clinical education and L&D teams while keeping costs low? As the medical device industry continues to evolve and grow, it’s more important than ever for medical device companies to invest in learning and development ...
Patient Recruitment and Inclusivity - The Patient Perspective
Delve into key takeaways from the C3 Summit's patient engagement panel, where industry experts and leaders discuss the challenges, opportunities, and strategies in clinical trial diversity and centricity through a candid patient perspective. Gain insights into accessibility...
Harnessing the Power of Electronic Clinical Outcomes Assessments (eCOA) Technology
Digital technologies are reshaping rare disease studies, placing the question of data integrity firmly in the spotlight. In this recap from our C3 Summit Session titled Harnessing the Power of Electronic Clinical Outcomes Assessments (eCOA) Technology, we examine the impact of...
Anticipate Your Language Needs: The Ultimate Clinical Trial Translations Checklist
Explore the world of clinical product development and discover the pivotal role of accurate translations in global clinical trials. Empower your study teams to navigate language challenges, ensuring patient safety, regulatory compliance, and successful outcomes. Achieve these...
Walking the Tightrope: Navigating Patient Centricity and Burden in Modern Clinical Trials
Explore the evolution of clinical trials and the challenge of patient burden. Learn how to strike the right balance between patient-centricity and research data extraction....
Health Canada's XML Mandate: Pioneering the Future of Pharmaceutical Content
Discover how Health Canada's transition to XML-based templates is reshaping Canadian healthcare content management. Learn about the benefits of XML formats, phases of implementation, and the transformative potential for pharmaceutical companies. TransPerfect Life Sciences...
Leveraging Technology and Bridging Gaps for Enhanced Clinical Data Management
Discover how technology-driven solutions are bridging gaps in clinical data management. Learn about challenges, trends, and strategies to enhance efficiency and streamline workflows for successful clinical research....
Driving Success in Omnichannel Content Strategies for Global and Local Markets
During our session at NEXT Pharma Summit in Dubrovnik, we explored the crucial role of an effective omnichannel approach in life sciences marketing. Seamlessly integrating multiple channels while considering the needs of global and local affiliates can unlock opportunities to...
Navigating the Regulatory Landscape for Expanded Access Programs
Preview: Discover the world of expanded access programs (EAPs) and the dynamic regulatory environment they operate in. In this blog, we delve into the significance of EAPs, the evolving global regulations governing them, and the vital role they play in providing timely treatment...
The Role of Qualitative Interviews in Ensuring a Patient-Centered Approach to Clinical Trials
Discover how qualitative interviews (CE, CD, PE, EI) enhance clinical trials. Learn best practices for conducting patient-centered interviews and ensuring accurate, meaningful data. Trust TransPerfect Life Sciences for expert interviewers and top-quality translation and...
IMP Labeling: EU CTR Transition Considerations
The blog post explores the critical aspects of transitioning Investigational Medicinal Product (IMP) labeling from the EU Clinical Trial Directive (EU CTD) to the new EU Clinical Trial Regulation (EU CTR). ...
