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Template:RegDocument

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This is the approved revision of this page, as well as being the most recent.
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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 — 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status Validity status Current, Draft, Final not promulgated, Superseded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