Need Regulatory Help? Try Our Platform
Post your regulatory questions or request quotations from verified pharmaceutical consultants worldwide. Get matched with experts who specialize in your market.
January 9, 2026
Approximately 5 minutes
Register of Authorised Pharmaceutical Distribution Entities in Spain – AEMPS Catalogue
Register of Authorised Pharmaceutical Distribution Entities in Spain – AEMPS Catalogue
Purpose and Scope
The AEMPS Catalogue of Pharmaceutical Distribution Entities serves as the official public register of all authorised operators in the pharmaceutical distribution chain in Spain. It includes wholesale distributors, manufacturing laboratories authorised for distribution activities, import/export entities, and warehouses under customs control or supervision. The catalogue enhances transparency for healthcare professionals, patients, other authorities, and the public by allowing verification of an entity's authorisation status, scope of activities, and compliance with Good Distribution Practice (GDP) and related regulations. It supports the prevention of falsified medicines and ensures only legitimate operators participate in the distribution of human and veterinary medicines. Catálogo de entidades de distribución - AEMPS
Content of the Catalogue
The catalogue provides detailed information on each authorised entity, including:
- Company name and legal identification (NIF/CIF).
- Authorisation number and date of issue.
- Type of authorisation (e.g., wholesale distribution, import, customs-supervised storage).
- Scope of activities (national, EU/EEA, third-country imports/exports).
- Address(es) of authorised premises (storage sites, offices).
- Responsible person or Qualified Person details.
- GDP or GMP certification status (where applicable).
- Validity period and any restrictions or conditions.
Entries are categorised by entity type and updated in real time following authorisation, variation, suspension, or revocation decisions.
Access and Verification
- Public Access: The catalogue is freely accessible online via the AEMPS website without registration.
- Search Functionality: Users can search by company name, authorisation number, province, activity type, or keyword.
- Download Options: Full or filtered lists can be exported in standard formats for regulatory or business use.
- Verification Use: Pharmacies, hospitals, competent authorities, and patients can confirm the legitimacy of suppliers before transactions.
Regulatory Context
Inclusion in the catalogue requires prior authorisation from AEMPS (and customs authorities where relevant), successful GDP inspection (for distributors), and ongoing compliance monitoring. Unauthorised distribution activities are illegal and subject to enforcement actions. The catalogue aligns with EU requirements for transparency in the pharmaceutical supply chain and supports the Falsified Medicines Directive (2011/62/EU) objectives.
This public register strengthens confidence in the Spanish pharmaceutical distribution system, facilitates legitimate trade, and contributes to patient safety by enabling quick verification of authorised operators. The catalogue is continuously maintained and reflects the current status of all registered entities. Complete search tools, download options, and additional guidance are available directly on the AEMPS catalogue page. Catálogo de entidades de distribución - AEMPS
Ask Anything
We'll follow up with you personally.
Related Articles
Approximately 5 minutes
Pharmaceutical Distribution and Laboratory Authorisations in Spain – AEMPS Requirements
AEMPS regulates pharmaceutical distribution and laboratory activities in Spain, requiring specific authorisations for wholesale distribution, manufacturing laboratories, and control laboratories to ensure traceability, quality, and compliance with Good Distribution Practice (GDP) and Good Manufacturing Practice (GMP) standards across the supply chain.
Approximately 5 minutes
Good Distribution Practice for Medicinal Products in the EU – Spanish Implementation by AEMPS
AEMPS enforces EU Good Distribution Practice (GDP) guidelines in Spain for wholesale distributors of human medicines, requiring authorisation, robust quality systems, temperature-controlled storage, qualified personnel, and full traceability to prevent falsified medicines and ensure product quality throughout the supply chain.
Approximately 5 minutes
Customs-Controlled and Supervised Medicinal Product Warehouses in Spain – AEMPS Guidelines
AEMPS regulates warehouses under customs control or supervision in Spain for storage of imported medicinal products awaiting customs clearance or release, ensuring compliance with storage conditions, security, traceability, and Good Distribution Practice (GDP) principles to maintain medicine quality and prevent entry of falsified products.
Approximately 5 minutes
Register of Medicinal Product Intermediaries in Spain – AEMPS Public List
AEMPS maintains a public register of authorised intermediaries in the medicinal product distribution chain in Spain, listing brokers and other entities that negotiate or arrange transactions without holding stock, to ensure transparency, regulatory compliance, and prevention of falsified medicines in line with EU requirements.
Approximately 5 minutes
Verification of Legality of Suppliers and Customers in Pharmaceutical Distribution – AEMPS Guidance
AEMPS requires wholesale distributors in Spain to verify the legitimacy and authorisation status of suppliers and customers before transactions, using the public AEMPS catalogue and other registers, to prevent falsified medicines from entering the legitimate supply chain and ensure compliance with EU Falsified Medicines Directive obligations.