FREE ON-DEMAND WEBINAR

Avoiding the Top Pitfalls in MedTech Clinical Data Collection: 2025 Strategies for Success

Stay ahead of the curve in 2025 with best practices to optimize clinical data collection, enhance compliance, and streamline workflows in the evolving MedTech landscape.

As the MedTech industry evolves, so do the challenges in clinical data collection. Regulatory expectations are intensifying, trial complexity is growing, and the tools of yesterday — like Excel, Word, and Google Forms—no longer meet the demands of modern clinical trials.

Join us for our first webinar of 2025, where we’ll explore how to navigate these challenges and avoid the pitfalls that can impact your compliance, timelines, and trial success. This forward-looking session will equip you with the strategies and tools needed to address the unique challenges of the year ahead.

In this session, we’ll cover:

  1. Why General Tools Are Obsolete in 2025 – Learn why tools like Excel, Word, and Google Forms are not equipped to handle the regulatory, security, and scalability needs of modern clinical trials, and how purpose-built solutions provide a competitive edge.
  2. Practical strategies to optimize study management, maintain compliance, and enhance decision-making – Gain actionable insights into how modern tools and workflows can simplify complex trials, ensure adherence to evolving regulatory requirements, and empower your team with real-time data for faster, more informed decisions.
  3. The Future of Data Integration – Discover how API-driven platforms are reshaping clinical trial data collection by breaking down silos and enabling real-time insights.
  4. Managing Complexity in a Digital-First World – Explore strategies to handle concurrent studies, multi-language requirements, and custom workflows, all tailored for the complexities of 2025 trials.
  5. Empowering Teams with Real-Time Oversight and Role-Based Access – See how advanced tools ensure your team has the right access to the right data at the right time, boosting efficiency and maintaining data integrity.

Watch the Webinar

Pitfalls in clinical data collection in 2025
Who should attend?
  • Clinical Affairs Professionals and Management
  • Clinical Operations Professionals and Management
  • Regulatory Professionals and Management
  • Product Development and Lifecycle Management Leaders
Watch Now!  

Hosted by

1613252124071
SPEAKER:
RASMUS BLENDAL

Product Manager
Greenlight Guru

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MODERATOR:
CHRIS RUSH

Solutions Engineer,
Greenlight Guru

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About Greenlight Guru

Greenlight Guru is the leading connected, cloud-based platform purpose-built for MedTech companies. The end-to-end solution streamlines product development, quality management, and clinical data management by integrating cross-functional teams, processes, and data throughout the entire product lifecycle.

Greenlight Guru’s platform is used by organizations across the globe that are replacing their disjointed, legacy tools and solutions to bring life-changing products to people faster and with less risk.

Visit our homepage to learn more.

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