Electronic Clinical Outcome Assessments (eCOA) have become a critical component in modern clinical trials. By digitizing traditional paper-based assessments, eCOA improves data accuracy, enhances patient compliance, and streamlines data collection processes. However, implementing eCOA requires careful planning, particularly when translating and migrating paper-based COAs into digital formats. This article explores the best practices for eCOA implementation, including existing methodologies, expert opinions, and key recommendations to ensure successful electronic migration and translation of COAs.

Medical translation in clinical research management is a key step to ensure accurate and clear communication between researchers, participants, and regulatory bodies, especially in multi-national or multi-lingual studies conducted by a clinical research organization. It involves translating clinical trial documents, such as informed consent forms (ICFs), patient questionnaires, and study protocols, from one language to another while maintaining the integrity of medical terminology and meaning. Professional medical translation services are essential to avoid misunderstandings, ensure participant safety, and comply with local regulations in different countries where clinical research centers may operate. A skilled medical translator ensures that all participants, regardless of their language, can understand the study's purpose, procedures, risks, and their rights, ultimately contributing to the success of the clinical research management process.

Boston is a global hub for medical technology, driven by its prestigious universities, cutting-edge research institutions, and a strong biotech ecosystem. The city is home to both established leaders like Boston Scientific and innovative startups advancing AI, robotics, and digital health. With strong collaboration between academia, healthcare, and venture capital, Boston remains a key player in shaping the future of medtech.

What is localisation and why it matters in the Health technology industry?

13th Annual Outsourcing in Clinical Trials: Medical Devices Europe

The future of digital diagnostics is marked by advancements in artificial intelligence and innovative technologies that significantly enhance disease detection and patient care. This post explains how these developments improve diagnostic accuracy, reduce turnaround times, and facilitate personalized medicine. It also highlights the benefits for communities worldwide, including better health outcomes and increased access to essential services, while promoting sustainable healthcare systems through predictive and preventative care models.

This article presents the transformative impact of 3D printing in the medical field, with applications in orthopedics, pediatrics, radiology, and oncology, highlighting how custom implants, patient-specific models, and bioprinted tumor studies are revolutionizing patient care and treatment strategies. I also discuss best practices and the benefits of translating and localizing medical 3D printing technologies to ensure effective communication and implementation across diverse markets.

In this article, I explain the importance of translating medical device IFUs and user manuals accurately and why choosing a specialized medical translator can help your business penetrate a new market smoothly - such as France. Read more to explore the benefits of accurate translation services for medical device manufacturers.

Discover the essential steps for obtaining CE marking for medical devices in Europe and learn how classifications differ between the US and EU. Find answers to key questions such as: What are the regulatory requirements for medical devices in the EU? How can I determine my device's classification? What documentation is needed for CE marking?