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RTF Template

Chief Pharmaceutical Inspectorate

UNION FORMAT FOR A WHOLESALE DISTRIBUTION AUTHORISATION

Human medicinal products

1. Authorisation Number	:	NZOH.5100.33.2023.MG.4
2. Name of Authorisation Holder	:	Przedsiebiorstwo Dystrybucji Farmaceutycznej Slawex Sp. z o.o. (ORG-100038328 / LOC-100060303)
3. Address(es) of Site(s)	:	Ul. Dworcowa 3f, Myslowice, Slaskie, 41-404, Poland

4. Legally registered address of Authorisation Holder	:	Ul. Budowlana 28, Lublin, 20-469
5. Scope of authorisation	:	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 wholesale distribution authorisation	:	Confidential, Confidential
8. Signature	:
9. Date	:	2026-10-01
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: Przedsiebiorstwo Dystrybucji Farmaceutycznej Slawex Sp. z o.o.

(ORG-100038328 / LOC-100079403)

, Ul. Dworcowa 3f, Myslowice, Slaskie, 41-404, Poland

Human medicinal products

1. MEDICINAL PRODUCTS

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

1.2. without a Marketing Authorisation or registration in the EEA and intended for EEA market*

2. AUTHORISED WHOLESALE DISTRIBUTION OPERATIONS

2.1. Procurement

2.2. Holding

2.3. Supply

3. MEDICINAL PRODUCTS WITH ADDITIONAL REQUIREMENTS

3.1. Narcotic or psychotropic products**

3.2. Products requiring low temperature handling

3.2.1. Temperatures between 2 to 8 °C

3.2.2. Other temperatures: (please specify) temperatury od 8 °C do 15 °C

3.3. Other products: (please specify here or make a reference to Annex 5) produkty krwiopochodne, immunologiczne produkty lecznicze, cytostatyczne produkty lecznicze

*Art. 5 of Directive 2001/83/EC, Art. 83 of Regulation (EC) 726/2004 and Art. 110 of Regulation 2019/6.

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

Union Format for a Wholesale Distribution Authorisation	NZOH.5100.33.2023.MG.4
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