Template:RegDocument
From GxPlex
Revision as of 14:21, 4 June 2026 by Gxplex admin (talk | contribs) (Add SMW property annotations to RegDocument template)
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 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
| 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 â 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Validity status | Current, Draft, Final not promulgated, Superseded |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 |