Category:In Vitro Diagnostics: Difference between revisions
From GxPlex
Gxplex admin (talk | contribs) Setup A+B navigation  |
Gxplex admin (talk | contribs) Add SMW Description property  |
||
| (One intermediate revision by the same user not shown) | |||
| Line 1: | Line 1: | ||
{{#set: Description=Regulatory documents and references under IVDR (EU 2017/746).}} | |||
Pages in this category cover regulatory documents and references in the In Vitro Diagnostics (IVD) scope. | Pages in this category cover regulatory documents and references in the In Vitro Diagnostics (IVD) scope. | ||
| Line 21: | Line 22: | ||
* [[:Category:Traceability|Traceability]] | * [[:Category:Traceability|Traceability]] | ||
* [[:Category:Performance Evaluation|Performance Evaluation]] | * [[:Category:Performance Evaluation|Performance Evaluation]] | ||
[[Category:Themes and topics]] | |||
Latest revision as of 16:39, 19 June 2026
Pages in this category cover regulatory documents and references in the In Vitro Diagnostics (IVD) scope.
Documents
| Name | Status | Region | Version | |
|---|---|---|---|---|
| In Vitro Diagnostic Medical Devices Regulation (EU) 2017/746 | In Vitro Diagnostic Medical Devices Regulation (EU) 2017/746 | Current | EU | 2017/746, amended by 2022/1107 |
Browse by topic
Pages in category "In Vitro Diagnostics"
This category contains only the following page.
