Health Products Regulatory Authority
UNION FORMAT FOR A WHOLESALE DISTRIBUTION AUTHORISATION
1. Authorisation Number
:
W00401/00001
2. Name of Authorisation Holder
Shire Pharmaceuticals (Ireland) Limited
3. Address(es) of Site(s)
Block 2 & 3, Miesian Plaza, 50-58 Lower Baggot Street, Dublin 2, -, -, Ireland
4. Legally registered address of Authorisation Holder
Block 2 & 3, Miesian Plaza, 50-58 Baggot Street Lower, Dublin 2, -, -, Ireland
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
2020-08-31
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
SCOPE OF WHOLESALE DISTRIBUTION AUTHORISATION
Name and address of the site: Shire Pharmaceuticals (Ireland) Limited
, Block 2 & 3, Miesian Plaza, 50-58 Lower Baggot Street, Dublin 2, -, -, Ireland
1.1. with a Marketing Authorisation in EEA country(s)
1.3. without a Marketing Authorisation in the EEA and intended for exportation
2.1. Procurement
2.3. Supply
2.4. Export
3.1.2. Medicinal products derived from blood
3.1.3. Immunological medicinal products
3.3. Cold chain products(requiring low temperature handling)
3.4. Other products: Please see restrictions or clarifying remarks (for all users).
Any restrictions or clarifying remarks (for all users): 3.4.1 Prescription only medicinal products 3.4.3 Over the counter medicinal products for sale through pharmacies only 3.4.4 Unauthorised medicinal products 3.4.12 Exempt medicinal products 3.4.13 Biological products Not all of the contract wholesale distribution sites listed in Annex 2 are appropriately authorised to hold all of the medicinal product categories listed in Annex 1.
*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:
Updated
Union Format for a Wholesale Distribution Authorisation
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