Optimized for MedTech Clinical Studies
Greenlight Guru Clinical (formerly SMART-TRIAL) provides a comprehensive and compliant platform for the collection and management of clinical evidence, safety, and performance data. Designed specifically for medical device studies, this software eliminates the need for coding, simplifies setup processes, and excludes expensive pharma-centric features that may not be relevant to your needs.
Enhancing Testing Processes
Testimonials like Jacob Anders Roug, Technical Audiologist at Oticon, showcase how Greenlight Guru Clinical enables organizations to conduct better and faster tests, unlocking new opportunities in testing methodologies. This solution streamlines data collection, allowing for more efficient and effective clinical trials and studies.
Comprehensive Clinical Solutions
From document management to post-market clinical surveys, Greenlight Guru Clinical covers a wide range of clinical data collection needs. The platform offers features such as electronic case report forms, electronic patient reported outcomes, ad-hoc data collection, and more, ensuring that every aspect of your clinical study is efficiently managed and documented.
Robust Support and Resources
Greenlight Guru provides extensive resources to support users in maximizing the potential of their EDC software. From blogs and podcasts to webinars and customer stories, users can access valuable insights and industry best practices. Additionally, the platform offers tools like checklists, templates, and eBooks to aid in various aspects of clinical data management.
Focus on Compliance and Quality
With a mission centered around quality and compliance in the medical device industry, Greenlight Guru offers solutions that align with regulatory standards such as ISO guidelines and FDA requirements. The platform facilitates seamless adherence to quality management processes, ensuring that your clinical data collection meets all necessary standards and regulations.