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Information Messages
  • The WDA has been withdrawn, withdrawn date is: 2024-10-03
  • RTF Template


    Federal Agency for Medicines and Health Products

    UNION FORMAT FOR A WHOLESALE DISTRIBUTION AUTHORISATION


    1. Authorisation Number

    :

    1976 H

    2. Name of Authorisation Holder

    :

    ADC Logistics BVBA

    3. Address(es) of Site(s)

    :

    Abelebaan 60, Ranst, 2520, Belgium 




    4. Legally registered address of Authorisation Holder

    :

    Abelebaan 60, Ranst, 2520, Belgium

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

    :

    ANNEX 1

    6. Legal basis of authorisation

    :


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

    :

    Confidential, Confidential

    8. Signature

    :


    9. Date

    :

    2019-08-05

    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: ADC Logistics BVBA

    , Abelebaan 60, Ranst, 2520, Belgium   




    1. MEDICINAL PRODUCTS

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


    2. AUTHORISED WHOLESALE DISTRIBUTION OPERATIONS

       2.1. Procurement 

       2.3. Supply 

       2.4. Export 


    3. MEDICINAL PRODUCTS WITH ADDITIONAL REQUIREMENTS

         3.1.2. Medicinal products derived from blood 

         3.1.3. Immunological medicinal products 

         3.1.4. Radiopharmaceuticals (including radionuclide kits) 

       3.3. Cold chain products(requiring low temperature handling) 




    Any restrictions or clarifying remarks (for all users):  2.1.: Also procurement of medicinal products coming from countries of the European Economic Area (EEA) other than Belgium.
    3.3.: Authorized temperature for the cold chain : 2-8°C

    2.1.: Alsook het verkrijgen van geneesmiddelen uit landen van de Europese Economische Ruimte (EER) anders dan België.
    3.3.: Toegestane temperatuur voor de koude bewaring : 2-8°C



    *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:

    a more recent version exists








    Union Format for a Wholesale Distribution Authorisation

    1976 H


    Page 1





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