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Information Messages
  • The WDA has been withdrawn, withdrawn date is: 2026-03-19
    		•
    RTF Template


    Health Products Regulatory Authority

    UNION FORMAT FOR A WHOLESALE DISTRIBUTION AUTHORISATION

    Human medicinal products


    1. Authorisation Number

    :

    W11769/00001

    2. Name of Authorisation Holder

    :

    Pharmasave Holdings Limited

    (ORG-100016152 / LOC-100024935)

    3. Address(es) of Site(s)

    :

    Northwood Court 43, Northwood Park, Northwood, Dublin 9, D09 V184, Ireland 




    4. Legally registered address of Authorisation Holder

    :

    Northwood Court 43, Northwood Park, Northwood, Dublin 9, D09 V184, Ireland

    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

    :

    2022-10-05

    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: Pharmasave Holdings Limited

    (ORG-100016152 / LOC-100024935)

    , Northwood Court 43, Northwood Park, Northwood, Dublin 9, D09 V184, Ireland   



    Human medicinal products


    1. MEDICINAL PRODUCTS

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

    2. AUTHORISED WHOLESALE DISTRIBUTION OPERATIONS

       2.1. Procurement 

       2.3. Supply 


    3. MEDICINAL PRODUCTS WITH ADDITIONAL REQUIREMENTS

       3.3. Other products: (please specify here or make a reference to Annex 5) Please see restrictions or clarifying remarks (for all users).




    Any restrictions or clarifying remarks (for all users):  3.3.1 Prescription only medicinal products3.3.2 Medicinal products for general sale3.3.3 Over the counter medicinal products for sale through pharmacies only3.3.6 Parallel imported medicinal products authorised by Parallel Product Authorisation (PPA)3.3.7 Parallel imported medicinal product authorised by Dual Pack Registration (DPR)3.3.8 Parallel distributed centrally authorised medicinal products3.3.11 Exempt medicinal products






    Reason for Withdrawing:

    Withdrawal approved 05.03.26







    Union Format for a Wholesale Distribution Authorisation

    W11769/00001


    Page 1





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