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RTF Template

Health Products Regulatory Authority

UNION FORMAT FOR A WHOLESALE DISTRIBUTION AUTHORISATION

Human medicinal products

1. Authorisation Number	:	W11229/00001
2. Name of Authorisation Holder	:	Mcnallys Pharmacy 365 Limited (ORG-100035886 / LOC-100056810)
3. Address(es) of Site(s)	:	Main Street, Kingscourt, Co. Cavan, A82 V2V8, Ireland

4. Legally registered address of Authorisation Holder	:	Unit 1 Boyne Business Park, Greenhills Business Park, 66 A Newtown Road, Drogheda, A92 K38D
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	:	2026-07-24
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: Mcnallys Pharmacy 365

(ORG-100039519 / LOC-100062245)

, Main Street, Kingscourt, Co. Cavan, A82 V2V8, 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

2.1. Procurement

2.2. Holding

2.3. Supply

2.4. Export

3. MEDICINAL PRODUCTS WITH ADDITIONAL REQUIREMENTS

3.3. Other products: (please specify here or make a reference to Annex 5) N/A

Any restrictions or clarifying remarks (for all users): ,3.3.01 Prescription only medicinal products,3.3.02 Medicinal products for general sale,3.3.03 Over the counter medicinal products for sale through pharmacies only,3.3.04 Unauthorised medicinal products,3.3.06 Parallel imported medicinal products authorised by Parallel Product Authorisation (PPA),3.3.07 Parallel imported medicinal product authorised by Dual Pack Registration (DPR),3.3.08 Parallel distributed centrally authorised medicinal products,3.3.11 Exempt medicinal 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	W11229/00001
	Page 1

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