Content in German
The detailed company information on this page is provided in the original German language. You can use your browser's built-in translation feature to view it in English.
Right-click on the page and select "Translate to English" or use the translation icon in your browser's address bar.
Radio-Pharm GmbH & Co. KG Address & Contact
Radio-Pharm GmbH & Co. KG Overview
Radio-Pharm GmbH & Co. KG was founded in 2005 in Hamburg and has since established itself as a reputable pharmaceutical intermediary. The company deals with the mediation of pharmaceuticals and pharmaceutical products in both the German and European markets. At a time when the supply and distribution of pharmaceuticals are becoming increasingly complex, Radio-Pharm plays a central role as a specialized pharmaceutical trading intermediary that efficiently and transparently manages the entire process of pharmaceutical distribution.
Services and Products
Radio-Pharm coordinates pharmaceutical trading activities in accordance with § 52b of the Medicines Act (AMG). The company specializes in the implementation of GDP guidelines (Good Distribution Practice), which allows it to conduct transactions between pharmaceutical companies and their customers without holding its own inventory. This structure enables Radio-Pharm to focus entirely on mediation while meeting the high requirements of pharmaceutical regulation. In addition, the company offers extensive consulting and support services to ensure that all transactions comply with current regulatory standards.
Location Hamburg / Hamburg
The choice of Hamburg as a location is of great strategic importance for Radio-Pharm. Hamburg is not only an important trading place in Germany but also internationally recognized. The city provides an excellent infrastructure that is essential for the efficient handling of pharmaceutical supply chains. Proximity to several significant port facilities allows for quick international transport of pharmaceuticals, while existing networks of logistics and service companies ensure smooth processing of operations. In this globalized environment, Radio-Pharm can optimally offer its services and effectively meet the demands of its customers.
Special Features and Innovations
A central aspect of Radio-Pharm is the commitment to quality and safety in pharmaceutical supply. By forgoing in-house storage, efficiency is further increased, and the company can react more flexibly to market needs. Radio-Pharm has established a modern IT infrastructure that ensures seamless traceability of all pharmaceutical transactions. This transparency is not only a legal requirement but also a significant criterion for the trustworthiness and reliability expected by customers and partners.
Regulatory Classification
Radio-Pharm operates as a pharmaceutical intermediary and is subject to the strict regulations of the German Medicines Act (AMG) as well as EU directives. The company holds all the necessary licenses required for operation in the pharmaceutical sector. Additionally, the Radio-Pharm team ensures that all employees are continuously trained and informed about the latest legal provisions. This not only minimizes the risk of regulatory violations but also upholds the highest standards in pharmaceuticals.
Importance for the Region
Radio-Pharm's activities have a clear positive impact on the Hamburg region. As one of the leading companies in the pharmaceutical sector, Radio-Pharm contributes to job creation and strengthening the economic infrastructure. Furthermore, by collaborating with various local pharmaceutical companies and promoting innovative approaches in pharmaceutical distribution, sustainable economic growth in the region is fostered. Thus, Radio-Pharm has established itself not only as an important player in the international pharmaceutical market but also as a responsible partner actively contributing to economic development in Hamburg.
Other pharmaceutical intermediaries: Overview of Pharmaceutical Intermediaries | Pharmaceutical Wholesale | Pharmaceutical Companies
Frequently asked questions about Radio-Pharm GmbH & Co. KG
What is Radio-Pharm GmbH & Co. KG?
Radio-Pharm GmbH & Co. KG is a licensed pharmaceutical broker based in Hamburg. Pharmaceutical brokers trade in their own name without taking ownership of the medicines and must be registered with the competent authority.
What does a pharmaceutical broker do?
A pharmaceutical broker acts as an intermediary between the manufacturer and buyer of medicines without being physically involved in the delivery process. The activity requires a licence under § 52c AMG and is subject to GDP requirements.
How is Radio-Pharm GmbH & Co. KG regulated?
As a pharmaceutical broker, Radio-Pharm GmbH & Co. KG is registered with the competent German authority and is subject to the requirements of the Medicines Act (AMG) and the EU Good Distribution Practice (GDP) guidelines.
More Drug Brokers in Hamburg
Drug Brokers in Germany
Related areas in healthcare
Drug Brokers by location
About Drug Brokers
A medicine broker (Arzneimittelvermittler) is a business that arranges the purchase or sale of human medicines between manufacturers, wholesalers and buyers, acting as an intermediary without ever taking physical possession of or legal title to the products. This role is formally defined under Section 4(22b) of the AMG (German Medicinal Products Act). Medicine brokers play a role in international parallel trade and in secondary supply chains, but their activities are subject to strict legal requirements to prevent counterfeit medicines from entering the legitimate supply chain. In Germany, anyone wishing to act as a medicine broker must register with the competent authority of the relevant German federal state under Section 52b AMG. Registration requires a permanent business address in Germany or another EU member state, a designated responsible person, and a fully documented quality management system that meets the requirements of the EU Good Distribution Practice (GDP) guidelines for medicine brokers. Failure to register or to maintain the required quality system constitutes a criminal offence under German pharmaceutical law. The registration system ensures traceability and accountability throughout the supply chain. Medicine brokers must not procure medicines from unlicensed sources or supply non-authorised products. The GDP requirements specific to brokers include record keeping, complaint handling, recall procedures and counterfeiting detection. This directory lists all medicine brokers registered with German authorities under Section 52b AMG, with addresses and contact details.
Medicine Brokering in Germany: Legal Framework
Medicine brokering is a regulated activity in Germany and across the European Union, governed by the EU Falsified Medicines Directive (2011/62/EU) and its implementing measures, transposed into German law through amendments to the AMG. The formal definition of a medicine broker (Arzneimittelvermittler) is set out in Section 4(22b) AMG: a natural or legal person who arranges transactions involving medicinal products for human use between manufacturers, wholesalers and buyers, without themselves acquiring or supplying the products and without taking physical possession of them. This intermediary role distinguishes brokers from wholesalers. The registration requirement under Section 52b AMG was introduced specifically to increase transparency and traceability in the medicine supply chain, after investigations revealed that unlicensed brokers had been involved in the entry of substandard or falsified medicines into European supply chains. Germany's registration system requires brokers to notify the competent state authority before commencing operations and to maintain their registration as long as they are active.
GDP Quality System Requirements for Medicine Brokers
Although medicine brokers do not physically handle medicines, they are still required to operate a documented quality management system (QMS) under the EU GDP guidelines for brokers (2013/C 343/01, Part III). The QMS must cover several key areas: written procedures (SOPs) for all brokering activities, a system for verifying that all counterpart manufacturers and wholesalers hold the required licences, a complaints handling system for quality-related issues, a product recall procedure that can be activated even though the broker did not physically move the goods, record keeping for a minimum of five years for all brokered transactions, and procedures for detecting and reporting suspected falsified medicines to the competent authority. Brokers must not source from or supply to unlicensed parties. Regular self-inspections and, where relevant, external audits ensure the QMS remains effective. The competent state authority may inspect a broker's QMS as part of its oversight activities.
Medicine Brokering and Parallel Trade in the EU
Medicine brokering is closely associated with parallel trade (Parallelhandel) in the EU pharmaceutical market. Parallel trade occurs when an authorised medicine is purchased in an EU member state where its price is lower and resold in another member state where the price is higher, exploiting price differentials across the single market. Germany, as a large market with relatively higher medicine prices than some southern and eastern European member states, is a significant destination for parallel-traded medicines. Parallel importers must obtain a parallel import permit from BfArM or PEI for each product, ensuring the imported medicine is equivalent to the authorised German version. Medicine brokers can play a role in arranging these cross-border transactions. However, all parties in the parallel trade supply chain, including brokers, must comply with applicable GDP and registration requirements. The Falsified Medicines Directive's safety features (tamper-evident packaging and unique identifiers under the EU Falsified Medicines Verification System, EMVS) apply to all prescription medicines circulating in Germany.
Compliance and GDP Requirements for Brokers
Pharmaceutical brokers remain under strict regulatory oversight despite not handling products physically. A broker's GDP quality system must include procedures for order processing, supplier qualification, complaints management, recall management and self-inspections. All brokered medicinal products must originate from legal, officially approved sources; transaction documentation must be kept comprehensively and retained for at least five years. Suspected falsified medicines must be reported to the competent authority. The European Commission defined clear requirements for brokers without product ownership in GDP Guidelines 2013/C 343/01. Regular self-inspections and the designation of a Responsible Person (RP) are mandatory. Violations can result in deregistration and criminal consequences under the Medicines Act. The Sanoliste directory only lists brokers who were registered in accordance with Section 52b AMG at the time of their entry.
What does a medicine broker do?
A medicine broker, as defined under Section 4(22b) of the AMG (German Medicinal Products Act), arranges transactions in human medicines without taking ownership of the products or physically handling them. Brokers must be registered with the responsible authority and maintain a quality management system.
What registration does a medicine broker need?
Medicine brokers must register under Section 52b AMG with the responsible state authority. Requirements include an official business address in Germany and a documented quality system meeting GDP (Good Distribution Practice) standards.
Where can I find registered medicine brokers in Germany?
The competent state pharmaceutical supervisory authority in each federal state maintains a register of brokers registered under Section 52b AMG. Sanoliste provides a searchable overview of registered medicine brokers across Germany with contact details and addresses.
Why are medicine brokers regulated in Germany?
Regulation of medicine brokers in Germany is primarily aimed at preventing counterfeit and substandard medicines from entering the legitimate pharmaceutical supply chain. By requiring registration and a documented GDP quality system, authorities can trace the origin and movement of medicines arranged by brokers. This protects patients and ensures that only authorised medicines from authorised sources reach pharmacies and hospitals.
What are the GDP requirements for medicine brokers in Germany?
Under EU GDP guidelines (2013/C 343/01), medicine brokers must maintain a quality system that covers written procedures, complaint handling, product recall procedures, record keeping and measures to detect falsified medicines. They must only deal with manufacturers and wholesalers that hold the appropriate authorisations. These requirements apply equally to brokers registered in Germany under Section 52b AMG.
How does medicine brokering differ from pharmaceutical wholesale in Germany?
The key difference is physical possession. A pharmaceutical wholesaler (Pharmagrosshandel) physically stores and ships medicinal products and requires a wholesale dealer authorisation under Section 52a AMG. A medicine broker (Arzneimittelvermittler) never takes possession of the goods; it only acts as an intermediary arranging deals between other parties. Brokers require registration under Section 52b AMG rather than a full wholesale authorisation.