18 lines
624 B
Plaintext
18 lines
624 B
Plaintext
== The Project ==
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GxPlex was started to address the need for a transparent, traceable document management system tailored to medical device regulation.
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=== Background ===
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Regulatory documentation under MDR (EU 2017/745) and IVDR (EU 2017/746) requires structured, versioned, and approved records. GxPlex provides a wiki-based platform optimised for this workflow.
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=== Goals ===
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* Traceable document lifecycle from draft to approved
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* Full-text and property-based search across all documents
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* Role-based access for authors, reviewers, and administrators
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=== Status ===
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The project is currently in active development.
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