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Information Messages
  • The WDA has been withdrawn, withdrawn date is: 2025-04-15
  • RTF Template


    National Agency For The Safety Of Medicine And Health Products

    UNION FORMAT FOR A WHOLESALE DISTRIBUTION AUTHORISATION

    Human medicinal products


    1. Authorisation Number

    :

    2023_319_4_6_7

    2. Name of Authorisation Holder

    :

    Centre Specialites Pharmaceutiques

    (ORG-100008565 / LOC-100014787)

    3. Address(es) of Site(s)

    :

    2 Rue Du Petit Marteau, Moussy Le Neuf, 77230, France 




    4. Legally registered address of Authorisation Holder

    :

    76 Avenue Du Midi, Cournon D Auvergne, 63800

    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

    :

    2023-12-06

    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: Centre Specialites Pharmaceutiques

    (ORG-100008565 / LOC-100087354)

    , 2 Rue Du Petit Marteau, Moussy Le Neuf, 77230, France   



    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 

       2.2. Holding 

       2.3. Supply 

       2.4. Export 


    3. MEDICINAL PRODUCTS WITH ADDITIONAL REQUIREMENTS

         3.1.1. Narcotic or psychotropic products 

         3.1.2. Medicinal products derived from blood 

         3.1.3. Immunological medicinal products 

       3.3. Cold chain products(requiring low temperature handling) 




    Any restrictions or clarifying remarks (for all users):  -
    Dépositaire, wholesale distributor of pharmaceutical products other than medicinal products and of intermediate products, wholesale distributor for export (Public Health Code Article R.5124-2 4° 6° 7°)

    4° storage, wholesale distribution of not owned medicinal products, by order and on behalf of exploitants

    6° purchase, storage, distribution of intermediates wich undergoe further processing by an authorised manufacturer or products mentioned in Article L.4211-1 2° and 3°

    7° purchase, storage with a view to the export without modification of medicinal products other than investigational medicinal products and products mentioned in article L. 4211-1 2°, 3°, 5°

    3.1.1: limited to psychotropic products, excluding narcotics

    Signatory: Mrs Florence Descamps-Delesalle, head of pharmaceutical product inspection and counterfeiting fight department
    The ANSM does not issue hard copy of this authorisation.

    -----------

    Établissement dépositaire, distributeur en gros de produits pharmaceutiques autres que les médicaments et de produits intermédiaires, distributeur en gros à l'exportation (code de la santé publique art. R.5124-2 4° 6° 7°)

    4° stockage, distribution en gros et en l'état de médicaments dont il n'est pas propriétaire, d'ordre et pour le compte d'exploitants

    6° achat, stockage, distribution en gros et en l'état de produits intermédiaires destinés à une transformation ultérieure par un fabricant autorisé ou de produits cités à l'article L.4211-1 2°, 3°

    7° achat, stockage en vue de l'exportation en l'état de médicaments autres que des médicaments expérimentaux et de produits cités à l'article L.4211-1 2°, 3°, 5°

    3.1.1 : limité aux psychotropes, stupéfiants exclus

    Signataire: Mme Florence Descamps-Delesalle, chef du Pôle inspection des produits pharmaceutiques et lutte contre les fraudes.
    L'ANSM ne délivre pas de copie papier de cette autorisation.








    Reason for Withdrawing:

    replaced with authorisation 2025_106_1_2_4_6_7

    remplacée par l'autorisation 2025_106_1_2_4_6_7








    Union Format for a Wholesale Distribution Authorisation

    2023_319_4_6_7


    Page 1





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