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

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Featured Capabilities:

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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Florian Tolkmitt

Florian is founder of a clinical evaluation marketplace for authors and medical device manufacturers called Clinical-Evaluation.Report.

He has a background in medical device development and regulatory affairs and worked for Medical Device Consultancies and in industry before he decided to help manufacturers as a Freelance Consultant.

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Recent Posts

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Introducing Adaptable Quality Processes: custom fields, enhanced visibility, and easy exports
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The 5 key elements of an effective CAPA system
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Welcome Ultralight Labs to Greenlight Guru

Focus on the Work That Matters Most.

See how Greenlight Guru’s MedTech Suite can help you eliminate the repetitive, low-value tasks of your day-to-day with a personalized demo.

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