$349 FREE TOOL

GSPR Template

The GSPR section of EU MDR 2017/45 outlines essential safety and performance requirements that medical devices must meet in order to be sold in the EU market. These requirements ensure devices are safe and effective for their intended use, protecting patients, users, and others.

Ensuring early compliance with GSPR is crucial for expediting the Notified Body accreditation process, especially given the current high demand and lengthy review and audit times.

To support your compliance journey, we're giving you exclusive access to an 80-page GSPR Template that guides you through the necessary steps, streamlining your path to compliance and helping you avoid delays.

This powerful tool, originally priced at $349, is being offered to you for free by Cannon Quality Group, the developer of the tool and a trusted partner of Greenlight Guru. Download your free copy now!

This free tool can help you:

• Evaluate Your Compliance and Quickly Identify Gaps: Assess your current adherence to MDR requirements and streamline your documentation with minimal effort. Identify areas of technical and clinical strength and pinpoint where improvements are needed.
• Identify Areas for Improvement: Gain insights into areas of nonconformance and effectively prioritize efforts and resources, saving you time and money.
• Ensure MDR Compliance: By ensuring that your organization fully complies with MDR requirements, this tool can help protect your organization from costly compliance issues and prioritize patient safety and device performance as you bring your device to market.