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RTF Template


Health Products Regulatory Authority

UNION FORMAT FOR A WHOLESALE DISTRIBUTION AUTHORISATION

Human medicinal products


1. Authorisation Number

:

W00190/00002

2. Name of Authorisation Holder

:

Pinewood Laboratories Limited

(ORG-100001380 / LOC-100000597)

3. Address(es) of Site(s)

:

Unit 1, M50 Business Park, Ballymount Avenue, Dublin 12, D12 K6C5, Ireland 




4. Legally registered address of Authorisation Holder

:

Ballymacarbry, Clonmel, E91 D434

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

:

2025-04-22

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: Pinewood Laboratories Limited

(ORG-100001380 / LOC-100007625)

, Unit 1, M50 Business Park, Ballymount Avenue, Dublin 12, D12 K6C5, Ireland   



Human medicinal products


1. MEDICINAL PRODUCTS

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

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

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


2. AUTHORISED WHOLESALE DISTRIBUTION OPERATIONS

   2.2. Holding 


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 only3.3.4 Unauthorised medicinal products3.3.11 Exempt medicinal products3.3.12 Biological products



*Art. 5 of Directive 2001/83/EC, Art. 83 of Regulation (EC) 726/2004 and Art. 110 of Regulation 2019/6.













Union Format for a Wholesale Distribution Authorisation

W00190/00002


Page 1





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