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Product Lifecycle Management (PLM)

MedTech

Closed-Loop Quality

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Explore the essentials of a Medical Device Quality Management System (QMS), ensuring safety, effectiveness, and compliance throughout the product lifecycle.

Read this blog post to understand what failure mode and effects analysis (FMEA) is and how it fits into Six Sigma.

Learn why you should institute corrective and preventative action in the pharmaceutical industry.

Implementing a corrective and preventative action (CAPA) plan is critically important for resolving product issues in the field and ensuring they don't happen again. Learn more.