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RTF Template

Bulgarian Drug Agency

UNION FORMAT FOR A WHOLESALE DISTRIBUTION AUTHORISATION

Human medicinal products

1. Authorisation Number	:	BG/WDA/MP-0642
2. Name of Authorisation Holder	:	Pharma Consult Bulgaria OOD (ORG-100038581 / LOC-100060620)
3. Address(es) of Site(s)	:	район Овча купел, ж.к. „Горна Баня", ул. „Вечерница" № 16 /, region Ovcha kupel, district Gorna Banya, 16 Vechernitsa str., гр. София / Sofia, 1614, Bulgaria

4. Legally registered address of Authorisation Holder	:	Ulitsa Vechernitsa 16, Gorna Banya, Oblast Sofia Grad, 1614
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	:	2026-05-12
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: PHARMA CONSULT BULGARIA LTD

, район Овча купел, ж.к. „Горна Баня", ул. „Вечерница" № 16 /, region Ovcha kupel, district Gorna Banya, 16 Vechernitsa str., гр. София / Sofia, 1614, Bulgaria

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

3.2. Products requiring low temperature handling

3.2.1. Temperatures between 2 to 8 °C

3.3. Other products: (please specify here or make a reference to Annex 5) Medicinal products derived from blood and immunological medicinal products лекарствени продукти, получени от кръв и имунологични лекарствени продукти

*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	BG/WDA/MP-0642
	Page 1

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