Template:RegDocument
From GxPlex
Template:RegDocument
Use this template on any page that documents a regulatory document (regulation, directive, guideline, treaty, scientific article, etc.).
Place the template call at the top of the page, before any prose content.
Usage
Copy and paste the block below, then fill in the values:
{{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Validity status | Current, Draft, Final not promulgated, Superseded |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 |