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RTF Template

Federal Agency For Medicines And Health Products

UNION FORMAT FOR A WHOLESALE DISTRIBUTION AUTHORISATION

Veterinary medicinal products

1. Authorisation Number	:	561 V
2. Name of Authorisation Holder	:	Antwerps Distributie Centrum (ORG-100022545 / LOC-100089991)
2.a. Alternative name of authorisation holder (optional)	:	Antwerps Distributie Centrum N.V.
3. Address(es) of Site(s)	:	Boechoutsesteenweg 17, Hove, 2540, Belgium Blauwesteenstraat 93-95, Kontich, 2550, Belgium

4. Legally registered address of Authorisation Holder	:	Blauwesteenstraat 95, Kontich, 2550
5. Scope of authorisation (complete for each site under 4)	:	ANNEX 1
6. Legal basis of authorisation	:	Art. 99 of Regulation (EU) 2019/6
7. Name of responsible officer of the competent authority of the member state granting the wholesaling authorisation	:	Confidential, Confidential
8. Signature	:
9. Date	:	2024-03-22
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: Antwerps Distributie Centrum

(ORG-100022545 / LOC-100035651)

, Boechoutsesteenweg 17, Hove, 2540, Belgium

Veterinary medicinal products

1. MEDICINAL PRODUCTS

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

2. AUTHORISED WHOLESALE DISTRIBUTION OPERATIONS

2.2. Holding

Name and address of the site: Antwerps Distributie Centrum

(ORG-100022545 / LOC-100073445)

, Blauwesteenstraat 93-95, Kontich, 2550, Belgium

Veterinary medicinal products

1. MEDICINAL PRODUCTS

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

2. AUTHORISED WHOLESALE DISTRIBUTION OPERATIONS

2.1. Procurement

2.2. Holding

2.3. Supply

2.4. Export

3. MEDICINAL PRODUCTS WITH ADDITIONAL REQUIREMENTS

3.1.1. Narcotic or psychotropic products

3.1.2. Medicinal products derived from blood

3.1.3. Immunological medicinal products

3.3. Cold chain products(requiring low temperature handling)

Any restrictions or clarifying remarks (for all users): 3.3.: Authorized temperature for the cold chain : 2-8°C

3.3.: Toegestane temperatuur voor de koude bewaring :2-8°C

*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

Union Format for a Wholesale Distribution Authorisation	561 V
	Page 1

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