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Information Messages
  • The WDA has been withdrawn, withdrawn date is: 2026-04-07
  • RTF Template


    Finnish Medicines Agency

    UNION FORMAT FOR A WHOLESALE DISTRIBUTION AUTHORISATION

    Human medicinal products


    1. Authorisation Number

    :

    FIMEA/2025/002283-2

    2. Name of Authorisation Holder

    :

    Grindeks Kalceks Suomi Oy

    (ORG-100050285 / LOC-100087775)

    3. Address(es) of Site(s)

    :

    Lonnrotinkatu 5, Helsinki, 00120, Finland 




    4. Legally registered address of Authorisation Holder

    :

    Lonnrotinkatu 5, Helsinki, 00120

    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

    :

    2025-04-24

    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: Grindeks Kalceks Suomi Oy

    (ORG-100050285 / LOC-100087775)

    , Lonnrotinkatu 5, Helsinki, 00120, 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 

       2.3. Supply 

       2.5. Other activities(s): (please specify) Distribution of medicinal product samples and export to other EEA countries


    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 





    *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.






    Reason for Withdrawing:

    New WDA issued, Authorisation Number: FIMEA/2026/001806-2








    Union Format for a Wholesale Distribution Authorisation

    FIMEA/2025/002283-2


    Page 1





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