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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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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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FDA's Proposed Wound Dressing Rule: Industry Impacts & Regulatory Insights
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Post-Market Surveillance for Medical Devices & IVDs: Requirements & Proactive Data Collection
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Data Management and Reporting in FDA-Regulated Clinical Trials

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