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RTF Template


Landesverwaltungsamt Sachsen-Anhalt

UNION FORMAT FOR A WHOLESALE DISTRIBUTION AUTHORISATION

Human medicinal products


1. Authorisation Number

:

DE_ST_01_WDA_2023_011

2. Name of Authorisation Holder

:

Strehlow GmbH

(ORG-100035737 / LOC-100056599)

3. Address(es) of Site(s)

:

Havelstrasse 23, Rothensee, Magdeburg, Saxony-Anhalt, 39126, Germany 




4. Legally registered address of Authorisation Holder

:

Havelstrasse 23, Rothensee, Magdeburg, Saxony-Anhalt, 39126

5. Scope of authorisation (complete for each site under 4)

:

ANNEX 1

6. Legal basis of authorisation

:

Art. 77(1) of Directive 2001/83/EC

7. Name of responsible officer of the competent authority of the member state granting the wholesaling authorisation

:

Confidential, Confidential

8. Signature

:


9. Date

:

2023-05-30

10. Annexes attached

:

Annex 1 Scope of wholesale distribution authorisation

Annex 2 (Optional) Address(es) of contract wholesale distribution sites and their authorisation number

Annex 3 (Optional) Name(s) of responsible person(s)

Annex 4 (Optional) Date of Inspection on which authorisation was granted

Annex 5 (Optional) Additional provisions based on national requirements


ANNEX 1

SCOPE OF WHOLESALE DISTRIBUTION AUTHORISATION



Name and address of the site: Strehlow GmbH

(ORG-100035737 / LOC-100056599)

, Havelstrasse 23, Rothensee, Magdeburg, Saxony-Anhalt, 39126, Germany   



Human medicinal products


1. MEDICINAL PRODUCTS

   1.1. with a Marketing Authorisation in EEA country(s)


2. AUTHORISED WHOLESALE DISTRIBUTION OPERATIONS

   2.1. Procurement 

   2.2. Holding 

   2.3. Supply 


3. MEDICINAL PRODUCTS WITH ADDITIONAL REQUIREMENTS

   3.2. Medicinal gases 




Any restrictions or clarifying remarks (for all users):  National legal basis of the authorisation: Section 52a (1) German Drug Law (AMG)
ref. 1.1: only skin and hand disinfectants
ref. 2.1 and 2.3: trading partly as drop shipment; sale exclusively to doctors and hospitals
This WDA is based on the confirmed layout plan dated 30/05/2023.

Nationale Rechtsgrundlage der Erlaubnis: § 52a (1) Arzneimittelgesetz (AMG)
zu 1.1: nur Haut- und Händedesinfektionsmittel
zu 2.1 und 2.: Handel teilweise als Streckengeschäft; Abgabe ausschließlich an Krankenhäuser und Ärzte
Die Erlaubnis basiert auf dem bestätigten Grundrissplan vom 30.05.2023.



*Art 5 of Directive 2001/83/EC or Art 83 of Regulation EC/726/2004

**Without prejudice to further authorisations as may be required according to national legislation













Union Format for a Wholesale Distribution Authorisation

DE_ST_01_WDA_2023_011


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