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RTF Template


Finnish Medicines Agency

UNION FORMAT FOR A WHOLESALE DISTRIBUTION AUTHORISATION

Human medicinal products


1. Authorisation Number

:

FIMEA/2025/000016-4

2. Name of Authorisation Holder

:

Woikoski Oy

(ORG-100000890 / LOC-100009561)

3. Address(es) of Site(s)

:

Puurtajankatu 22, Jarvenpaa, 04440, Finland 




4. Legally registered address of Authorisation Holder

:

P. O. Box 1, Woikoski, 52020, Finland

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

:

2025-01-22

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: Woikoski Oy

(ORG-100000890 / LOC-100008747)

, Puurtajankatu 22, Jarvenpaa, 04440, Finland   



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 

   2.5. Other activities(s): (please specify) Export to other EEA countries, supply to patients and parties with retail distribution rights


3. MEDICINAL PRODUCTS WITH ADDITIONAL REQUIREMENTS

   3.3. Other products: (please specify here or make a reference to Annex 5) Medicinal gases




Any restrictions or clarifying remarks (for all users):  Export to other EEA countries is limited only to medicinal products that are not used in human or animal.



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













Union Format for a Wholesale Distribution Authorisation

FIMEA/2025/000016-4


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