Streamlined Product Management Activities
Greenlight Guru offers a solution to streamline product management activities in the journey to commercialization. By providing a connected system that enhances collaboration, ensures traceability, and makes crucial information visible, Greenlight Guru simplifies the complex process of bringing a medical device to market. With this platform, you can avoid unnecessary challenges and focus on achieving your commercialization goals efficiently.
End-to-End Software Solution
Instead of relying on outdated single-process systems that use paper or spreadsheets, Greenlight Guru provides an end-to-end software solution. This advanced system enables you to manage both development and quality aspects simultaneously, preventing you from being led down a riskier path by inadequate product development solutions or processes. With Greenlight Guru, you can ensure a comprehensive approach to managing your product development lifecycle.
Comprehensive Product Management Capabilities
Greenlight Guru's platform offers a wide range of product management capabilities to support your needs. From document management and design control to risk management, change management, training management, and CAPA (Corrective and Preventive Actions) management, Greenlight Guru covers all aspects of product development. Additionally, the platform supports complaint management, nonconformance handling, project management, audit management, supplier management, and product change management, providing a holistic solution for efficient product development.
Support for Clinical Processes
In addition to product development support, Greenlight Guru also caters to clinical processes within the medical device industry. With features like electronic case report forms, electronic patient-reported outcomes, ad-hoc clinical data collection, post-market clinical surveys, and other clinical add-ons, Greenlight Guru offers comprehensive tools to streamline clinical data management. This ensures that companies can effectively manage their clinical trials and studies while maintaining compliance and data integrity.