Q100588753
Swedish delegated legislation from 2009
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Q100588753
Summary
Q100588753 is an implementing regulation[1].
Key Facts
- Q100588753 is in the country of Sweden[2].
- Q100588753's instance of is recorded as implementing regulation[3].
- Q100588753's language of work or name is recorded as Swedish[4].
- Q100588753 was released on +2009-05-07T00:00:00Z[5].
- Q100588753's main subject is medication[6].
- Q100588753's main subject is Swedish Medical Products Agency[7].
- Q100588753's work available at URL is recorded as https://www.riksdagen.se/sv/dokument-lagar/dokument/_sfs-2009-392[8].
- Q100588753's work available at URL is recorded as http://data.riksdagen.se/dokument/sfs-2009-392[9].
- Q100588753's applies to jurisdiction is recorded as Sweden[10].
- Q100588753's legal citation of this text is recorded as SFS 2009:392[11].
- Q100588753's published in is recorded as Q100565329[12].
- Q100588753's title is recorded as Förordning (2009:392) om Läkemedelsverkets skyldigheter i fråga om medicintekniska produkter[13].
- Q100588753's repealed by is recorded as Q110576697[14].
- Q100588753's maintained by WikiProject is recorded as Project Riksdagen's documents[15].
- Q100588753's copyright status is recorded as public domain[16].
- Q100588753's effective date is recorded as +2010-03-21T00:00:00Z[17].
Body
Definition and Type
Q100588753's instance of is recorded as implementing regulation[3].