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More than a Quality Management System: Tools for the entire MedTech Lifecycle.

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Document Management Training Management Product Development Design Control Risk Management CAPA Management Audit Management

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Data collection and management designed for MedTech clinical trials.

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Featured Capabilities:

Electronic Data Capture (EDC) Electronic Case Report Forms (eCRF) Electronic Patient Reported Outcomes (ePRO) Ad-Hoc Data Collection (Cases) Post-Market Surveys Product Add-Ons

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Ultimate Guide to Comparing Quality Management System Solutions

This eBook compares the best QMS software solutions to help medical device companies make an informed decision when investing in a quality management system.

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ISO 13485 - Ultimate Guide to Quality Management System (QMS) for Medical Devices

UG ISO 13485

This ultimate guide offers industry professionals everything related to the topic of ISO 13485. Greenlight Guru's QMS software automates regulatory compliance with ISO 13485:2016, FDA, ISO 14971, so companies can focus on delivering high-quality devices to patients.

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