Featured Product
This Week in Quality Digest Live
FDA Compliance Features
Jill Roberts
Another way to know what’s too old to eat
Patricia Santos-Serrao
Four pharma quality trends
Del Williams
Preventing damage caused by large, suspended particles
Kari Miller
An effective strategy requires recruiting qualified personnel familiar with the process and technology

More Features

FDA Compliance News
Now is not the time to skip critical factory audits and supply chain assessments
Google Docs collaboration, more efficient management of quality deviations
Delivers time, cost, and efficiency savings while streamlining compliance activity
First trial module of learning tool focuses on ISO 9001 and is available now
Free education source for global medical device community
Good quality is adding an average of 11 percent to organizations’ revenue growth
Further enhances change management capabilities
Creates adaptive system for managing product development and post-market quality for devices with software elements
VQIP allows for expedited review and importation for approved applicants that demonstrate safe supply chains

More News


FDA Compliance

Greenlight Guru Updates Risk Management to Align With ISO 14971:2019

Further enhances change management capabilities

Published: Thursday, March 26, 2020 - 12:00

(Greenlight Guru: Indianapolis) -- Greenlight Guru, creator of the only quality management software designed specifically for the medical device industry, announces new software platform updates to align with the recently updated ISO 14971:2019 standard, as well as further enhancements to the change management capabilities that debuted in December 2019.

ISO 14971 is the predominant standard for risk management in the medical device industry, of which compliance is required in the United States, Canada, and the European Union. Put into effect in December 2019, ISO 14971:2019 is the latest update to the application of risk management for medical devices. It serves to define better key terminology, residual risk identification, and personnel competence.

“This iteration of the ISO 14971 standard is the first update in nearly 13 years, and offers much-needed clarifications to reflect current best practices,” says Jon Speer, founder and vice president of QA/RA at Greenlight Guru. “The update to our platform not only conforms to the new standard but represents our continued dedication to being the best quality management system for medical device companies.”

Greenlight Guru’s timely platform update to help medical device companies comply with these changing regulatory standards is proof that they eliminate the burden of allocating internal resources to update the design and quality processes for customers, allowing them to stay current with evolving industry regulations and compliance requirements.

Updates to the Greenlight Guru platform reflects changes to align with ISO 14971:2019, as well as several productivity enhancements, including:
• Enhanced change management capabilities intended to assure medical device companies are systematically assessing the impact of changes through built-in change evaluation functionality
• The debut of Group Management, which gives companies the flexibility to create and manage different groups of employees based on how their teams or organization are uniquely structured

This announcement comes on the heels of significant enhancements to Greenlight Guru’s change management workflows, the launch of Digital Design Reviews, and the company’s fifth consecutive quarter as a G2 Crowd market leader in the quality management software category.

For more information about Greenlight Guru’s risk management capabilities, visit www.greenlight.guru/risk-management-software.


About The Author

greenlight.guru’s picture


Greenlight Guru is the only quality management software designed specifically for the medical device industry.