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November 1, 2018

Medical device solutions firm Greenlight Guru integrates with Jira

US-based Greenlight Guru, a medical device quality management software provider, has integrated its platform with issue and project tracking tool Jira.

US-based Greenlight Guru, a medical device quality management software provider, has integrated its platform with issue and project tracking tool Jira.

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Medical device companies can use the integrated system to manage product development and post-market quality for their software-based devices.

Greenlight added that the combined platform will allow companies to minimise non-compliance risk by ensuring the capture of relevant Jira artefacts in their quality management system.

“Medical device companies can use the integrated system to manage product development and post-market quality for their software-based devices.”

Greenlight Guru Quality Assurance and Regulatory Affairs co-founder and vice-president Jon Speer said: “Modern medical devices contain hardware, software and firmware levels, each of which is commonly owned and developed by cross-functional teams.

“This integration allows product managers to track and maintain compliance mandated by regulatory bodies while enabling software development in one of the most popular and adaptable management environments in the industry.”

Software development teams can also use Jira’s agile functionality to track implementation work and issues associated with software components.

It also facilitates simultaneous traceability to their design control and risk management system of record within Greenlight.

Greenlight Guru co-founder and CEO David DeRam added: “The agile development approach has helped bring about world-class technology like Gmail, Spotify and Salesforce.

“Greenlight Guru and Jira are the industry leaders in their respective fields; and, this new partnership will help usher in the next generation of quality-focused medical devices to market.”

The firm’s quality management software platform has been specifically designed for medical device companies. It is said to aid companies in obtaining safer products and simplify regulatory compliance.

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Free Report
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Medical Device Industry Landscape In Asia-Pacific

GlobalData's APAC Medical Devices Industry Landscape – 2022 free study breaks down the APAC medical devices market by segment and region and includes insights on local and global competitors, pipeline product developments, clinical trials studies, and significant deals in the industry. The APAC medical device industry witnessed significant developments, launches, implementations, and adoption of new medical device technologies in the past decade, however the high cost of devices, regulatory hurdles, reimbursement pressure, and healthcare budget constraints have challenged market expansion across various territories and segments. APAC is the fastest growing regional market for medical device clinical trials, with China and Japan emerging as major clinical trial hotspots. The growth in medical device clinical trials in the APAC region is attributed to an increase in research partnerships between biopharma companies and clinical research organizations (CROs). This report also provides an in-depth analysis of the medical device market's opportunities and challenges, the influence of COVID-19 on the market, and government activities aimed to develop the APAC medical device market.
by GlobalData
Enter your details here to receive your free Report.

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