Streamlining Software Validation
Greenlight Guru offers a modern solution for medical device software validation, addressing the challenges faced by MedTech companies in this critical process. Software validation can be complex and time-consuming, but with Greenlight Guru, companies can streamline this process and ensure their teams meet evolving validation requirements. By providing a premium experience and valuable resources, Greenlight Guru allows teams to focus more on utilizing the software effectively and less on testing it.
Comprehensive Product Features
Greenlight Guru's medical device software validation solution covers a wide range of features to support quality and compliance in the industry. From document management and product development to design control, risk management, change management, and more, the platform offers a comprehensive suite of tools to address various aspects of medical device software validation. With functionalities such as training and CAPA management, complaint handling, nonconformance resolution, and project and audit management, Greenlight Guru enables companies to navigate the validation process efficiently.
Resourceful Support and Guidance
In addition to its robust product features, Greenlight Guru provides extensive resources to assist companies in achieving successful software validation. The platform offers an ROI calculator to quantify the benefits of using Greenlight Guru, along with a wealth of educational materials such as blogs, podcasts, webinars, and customer stories. By offering checklists, templates, eBooks, and guides, Greenlight Guru equips users with the necessary knowledge and tools to streamline validation processes, stay compliant, and drive efficiency across their operations.
Industry-Leading Compliance
With a focus on ensuring regulatory compliance and quality management, Greenlight Guru stands out as an industry leader in medical device software validation. The platform supports various regulatory standards such as ISO 13485, ISO 14971, ISO 14155:2020, 21 CFR Part 820, and 21 CFR Part 11, enabling companies to adhere to key requirements and maintain a high level of quality within their operations. By guiding companies through essential processes like design controls, CAPA, and IQ, OQ, PQ, Greenlight Guru helps organizations achieve and sustain compliance effectively.