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GxPlex Search: Difference between revisions

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fix: complete search page – InputBox, sortable document table, topic browse, filter reference
Replace static ask table with dynamic filter UI placeholder
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=== All documents ===
=== Filter documents ===


All regulatory documents currently in this wiki. Click any column header to sort.
<div id="gplx-search-app">Loading search…</div>
Β 
{{#ask: [[Status::+]]
| ?Document name = Document
| ?Scope = Scope
| ?Area of validity = Region
| ?Document type = Type
| ?Status = Status
| ?Language = Language
| ?Restricted access = Restricted
| format=table
| headers=show
| limit=500
| tableclass=wikitable sortable
| sort=Document name
| order=asc
}}


=== Browse by topic ===
=== Browse by topic ===
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|-
|-
| [[:Category:Traceability|Traceability]] || UDI systems and device identification obligations under MDR and IVDR
| [[:Category:Traceability|Traceability]] || UDI systems and device identification obligations under MDR and IVDR
|}
=== Advanced filter ===
Use [[Special:Ask]] to combine multiple filters in one query. Available filter properties:
{| class="wikitable"
! Property !! Example values
|-
| <code>Area of validity</code> || EU, USA, Global, DE
|-
| <code>Scope</code> || MD, IVD, GMP, GEP, NIS, PV, IMP
|-
| <code>Document type</code> || Regulation, Directive, Guideline, Scientific article, Treaty
|-
| <code>Status</code> || Current, Draft, Final not promulgated, Superseded
|-
| <code>Language</code> || EN, DE, FR
|-
| <code>Restricted access</code> || Yes, No
|}
|}

Revision as of 16:55, 23 June 2026

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Topic Description
Medical Devices Regulatory documents and references under MDR (EU 2017/745)
In Vitro Diagnostics Regulatory documents and references under IVDR (EU 2017/746)
EU Regulation Core EU regulatory frameworks covering medical devices and IVDs
Clinical Clinical evaluation, clinical performance studies, PMCF, and PMPF
Labelling Labelling requirements, UDI carriers, and packaging obligations
Post-Market Surveillance PMS plans, PMCF, PMPF, and periodic safety update reports
Performance Evaluation Performance evaluation plans, reports, and PMPF for IVD devices
Traceability UDI systems and device identification obligations under MDR and IVDR
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