== Template:RegDocument ==
Use this template on any page that documents a regulatory document. Place it at the top of the page before any prose content.
This template also annotates each field as a [[Help:Semantic MediaWiki|Semantic MediaWiki]] property, enabling structured queries across all document pages.
=== Usage ===
{{RegDocument
| area_of_validity =
| scope =
| document_type =
| name =
| version =
| source =
| language =
| status =
| restricted_access =
}}
=== Fields ===
{| class="wikitable"
! Field !! Description !! Example values
|-
| area_of_validity || Region or country where the document applies || EU, USA, Global, DE
|-
| scope || Regulatory scope(s), comma-separated || MD, IVD — or NIS, GMP, PV, IMP, GEP, HM
|-
| document_type || Type of document || Regulation, Directive, Guideline, Scientific article, Treaty
|-
| name || Full official document name || Medical Device Regulation (EU) 2017/745
|-
| version || Version, revision or amendment || 2017/745, amended by 2023/607
|-
| source || URL to the official source || https://eur-lex.europa.eu/...
|-
| language || Available language(s) || EN, DE, FR
|-
| status || Validity status || Current, Draft, Final not promulgated, Superseded
|-
| restricted_access || Blocks copy/paste of content, referencing still allowed || Yes / No
|}
[[Category:Templates]]