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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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Jason Lim

Jason Lim is the CEO & Co-founder of Yeng & Leong MedTech Consultancy where they help companies establish quality management system (QMS) compliant to medical device industry standards and provide guidances necessary for navigating through the global regulatory landscape. They work with their international partners for regulatory, clinical and manufacturing support to provide our clients a comprehensive, one-stop solution so that medical devices are on track to being approved for sale in target markets.

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Recent Posts

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The 5 most common clinical data pitfalls in 2025 (and how to avoid them)
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Facing uncertainty: how medical device companies are navigating the current economic conditions
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Introducing Document Comparison: Boost Audit Readiness, Accelerate Training, and Streamline Approvals

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