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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 Supplier 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 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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checklists and templates

Checklist: 7 Steps to Comply with FDA 21 CFR Part 11

Checklist_ 7 Steps to Comply with FDA 21 CFR Part 11 - slide-in cover

A free checklist with seven steps that medical device companies can follow to ensure compliance with FDA 21 CFR Part 11.

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