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Information Messages
  • The WDA has been withdrawn, withdrawn date is: 2024-10-15
  • RTF Template


    State Agency Of Medicines

    UNION FORMAT FOR A WHOLESALE DISTRIBUTION AUTHORISATION

    Human medicinal products


    1. Authorisation Number

    :

    935

    2. Name of Authorisation Holder

    :

    Novo Nordisk Estonia OÜ

    (ORG-100049136 / LOC-100082897)

    3. Address(es) of Site(s)

    :

    Paldiski Mnt 29, Kristiine Linnaosa, Tallinn, 10612, Estonia 




    4. Legally registered address of Authorisation Holder

    :

    Paldiski Mnt 29, Kristiine Linnaosa, Tallinn, 10612

    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

    :

    2023-09-01

    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: Novo Nordisk Estonia OÜ

    (ORG-100049136 / LOC-100082897)

    , Paldiski Mnt 29, Kristiine Linnaosa, Tallinn, 10612, Estonia   



    Human medicinal products


    1. MEDICINAL PRODUCTS

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

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

       1.3. without a Marketing Authorisation in the EEA and intended for exportation


    2. AUTHORISED WHOLESALE DISTRIBUTION OPERATIONS

       2.1. Procurement 

       2.3. Supply 

       2.4. Export 


    3. MEDICINAL PRODUCTS WITH ADDITIONAL REQUIREMENTS

       3.3. Cold chain products(requiring low temperature handling) 





    *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






    Reason for Withdrawing:

    Due to responsible person change the date of issue was changed to be compliant with national WDA date (24.09.2024 nr KTM-7/24/107). New WDA with a new date has been issued.








    Union Format for a Wholesale Distribution Authorisation

    935


    Page 1





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