Eumedica Pharmaceuticals GmbH
Pharmaceutical Companies · Lörrach
Eumedica Pharmaceuticals GmbH is a pharmaceutical company based in Lörrach, Baden-Württemberg, Germany. The company operates in the German pharmaceutical market and is regulated by the BfArM (Federal Institute for Drugs and Medical Devices).
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Eumedica Pharmaceuticals GmbH Address & Contact
Eumedica Pharmaceuticals GmbH Overview
Eumedica Pharmaceuticals GmbH is the German subsidiary of the Belgian Eumedica S.A. and is based in Lörrach, Baden-Württemberg. The company specializes in the development and distribution of intravenous and inhalative specialty pharmaceuticals. The location in Lörrach, near the borders of Switzerland and France, offers a favorable position within the European pharmaceutical distribution network. This regional location allows for not only quick access to various markets but also promotes cooperation with international healthcare partners.
Field of Activity & Products
Eumedica has established itself as an important player in the field of intensive medicine and specialty therapies. The company's best-known product is Choledyl (Choline-Theophylline), which is primarily used for the treatment of respiratory diseases. In addition to this medication, Eumedica distributes a variety of other products tailored to specific clinical needs. These include, among others, medications for the treatment of cardiovascular diseases and analgesics for surgical procedures.
The company serves hospitals and specialist physicians not only in Germany but also in other European markets. Through targeted research and development, Eumedica creates innovative pharmaceuticals that are clearly aimed at the special requirements of clinical practice. Distribution is carried out via a well-developed network that guarantees both quicker access to products and continuous medical support for users.
Regulation
Eumedica Pharmaceuticals GmbH, as a pharmaceutical dealer and importer, is subject to the requirements of the German Medicines Act (AMG) and the EU directives for pharmaceutical companies. The company is registered with the Federal Institute for Drugs and Medical Devices (BfArM) and is supervised by the Freiburg District Government. These regulatory frameworks ensure that the products meet high-quality standards and that patient safety is guaranteed at all times.
Additionally, Eumedica holds all necessary certifications to meet the requirements for drug production and importation. The focus on quality and safety is underscored by regular audits and inspections by both internal and external auditors. Thus, Eumedica aims not only to comply with legal regulations but also to provide real added value to the healthcare sector.
Regional Significance
Eumedica Pharmaceuticals GmbH plays a significant role in regional healthcare provision. Due to its geographical proximity to large metropolitan areas as well as various medical institutions in Germany, Switzerland, and France, the company is able to respond quickly to changes in the healthcare sector. This not only supports the availability of specialty pharmaceuticals but also fosters exchange with medical professionals.
In Lörrach itself, Eumedica is also an important employer and offers numerous jobs in various fields, from research and development to production and sales. The company actively contributes to the social and economic development of the region by partnering with local educational and research institutions.
Special Features and Innovations
Eumedica is characterized by its focus on research and development of innovative pharmaceuticals. The company continuously invests in clinical studies to further optimize the efficacy and safety of its products. An ongoing project currently in the pipeline focuses on the further development of formulations for inhalative medications to improve the patient experience.
Moreover, the company participates in international research initiatives to integrate new insights and technologies into product development. Eumedica is also actively engaged in patient education and therefore offers training for medical professionals to ensure the safe handling of its pharmaceuticals.
More information: Pharmaceutical companies in Baden-Württemberg or all pharmaceutical companies in Germany on Sanoliste.
Frequently asked questions about Eumedica Pharmaceuticals GmbH
What does Eumedica Pharmaceuticals GmbH do?
Eumedica Pharmaceuticals GmbH is a pharmaceutical company based in Lörrach that develops, manufactures or distributes pharmaceutical products. The company is active in the German healthcare market.
Where is Eumedica Pharmaceuticals GmbH located?
Eumedica Pharmaceuticals GmbH is headquartered in Lörrach, Germany. More information can be found on the company's website.
What products does Eumedica Pharmaceuticals GmbH distribute?
Eumedica Pharmaceuticals GmbH is active in the pharmaceutical sector. Detailed information on the products offered and therapeutic areas can be found on the company's website or via the contact details provided.
Eumedica Pharmaceuticals GmbH on social media
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About Pharmaceutical Companies
Germany is one of the world's leading pharmaceutical nations, home to more than 1,000 pharmaceutical businesses employing approximately 130,000 people (vfa 2023). Companies operating in this sector develop, manufacture and distribute medicines across the entire value chain, from early-stage research and clinical trials through to market authorisation and commercial distribution. In Germany, every manufacturer of medicinal products must hold a manufacturing authorisation (Herstellungserlaubnis) issued under Section 13 of the AMG (Arzneimittelgesetz, Germany's Medicinal Products Act). Medicines may only be placed on the market after receiving approval from either BfArM (Bundesinstitut für Arzneimittel und Medizinprodukte, Germany's Federal Institute for Drugs and Medical Devices, broadly comparable to the FDA in the United States or the MHRA in the United Kingdom) or the European Medicines Agency (EMA) via the centralised procedure. All manufacturing sites are subject to regular GMP (Good Manufacturing Practice) inspections carried out by the competent pharmaceutical supervisory authority of the relevant German federal state. The sector covers prescription-only medicines (Rx), non-prescription OTC products, generics, biosimilars and active pharmaceutical ingredients (APIs). This directory lists pharmaceutical manufacturers, marketers and licence holders across all German federal states with full contact details, addresses and phone numbers.
Germany's Pharmaceutical Industry
Germany is consistently ranked among the top five pharmaceutical markets worldwide, generating annual revenues exceeding EUR 50 billion and accounting for the largest share of pharmaceutical production in continental Europe. The industry is represented by two major associations: vfa (Verband Forschender Arzneimittelhersteller), which represents research-based companies, and BAH (Bundesverband der Arzneimittel-Hersteller), which represents the broader manufacturer base including OTC and self-medication products. German pharmaceutical companies cover the full spectrum from global innovator corporations and mid-sized specialty manufacturers to generic producers and biotech firms. The country is a world leader in active pharmaceutical ingredient (API) production, biologics manufacturing and pharmaceutical chemistry. Key therapeutic areas of strength include oncology, cardiovascular medicine, immunology, neuroscience and rare diseases. Germany also serves as a significant export hub, with pharmaceutical products among the country's leading export categories. The sector benefits from a highly skilled workforce, world-class university research institutions and a dense network of research hospitals (Universitätsklinika) that facilitate clinical trial activity.
Regulatory Framework: BfArM, EMA and the AMG
The legal foundation for pharmaceutical activity in Germany is the Arzneimittelgesetz (AMG, German Medicinal Products Act), which regulates the authorisation, manufacture, import, distribution, labelling and pharmacovigilance of medicinal products. For English-speaking readers unfamiliar with the German regulatory landscape: BfArM (Bundesinstitut für Arzneimittel und Medizinprodukte) is the national competent authority responsible for approving medicines marketed only in Germany, supervising narcotics, and maintaining the pharmacovigilance database. BfArM is a higher federal authority (Bundesoberbehörde) subordinate to the Federal Ministry of Health (Bundesministerium für Gesundheit). For medicines approved via the centralised EU procedure, the European Medicines Agency (EMA) grants a single marketing authorisation valid in all 27 EU member states. Germany is also home to the Paul-Ehrlich-Institut (PEI), a second federal authority that specifically handles biological medicines including vaccines, blood products and gene therapy products. Manufacturing sites are inspected by state-level pharmaceutical supervisory authorities (Landesbehörden) to verify GMP compliance, with findings entered into the EudraGMDP database operated by the EMA.
Regional Pharmaceutical Clusters in Germany
Germany's pharmaceutical industry is geographically distributed across several major regional clusters. The Rhine-Main area around Frankfurt and Leverkusen in North Rhine-Westphalia is home to some of Germany's largest pharmaceutical sites, including facilities belonging to global corporations with long histories in German chemistry and pharmaceuticals. Bavaria (particularly Munich, Penzberg and Marburg) is a second major hub, especially strong in biotechnology and biologics production. Baden-Württemberg, including cities such as Mannheim, Heidelberg and Biberach an der Riss, is home to several significant research-based manufacturers. Hamburg and the northern German region have a cluster of specialty and generic manufacturers. Berlin has a growing biotech scene connected to its research universities and the Charité hospital. Hesse is notable for its proximity to Frankfurt's logistics infrastructure and several major API manufacturers. Smaller but significant clusters exist in Saxony (Leipzig, Dresden) and Lower Saxony, benefiting from proximity to university research centres and historically established chemical industry sites.
Drug Classes and Product Segments
German pharmaceutical companies cover all major drug classes. Prescription (Rx) products account for the largest share of revenue; generics manufacturers such as Stada, ratiopharm (Teva) and Hexal produce chemically equivalent alternatives after patent expiry, significantly reducing costs for the healthcare system. Biologics and biosimilars are gaining ground rapidly: monoclonal antibodies, insulin analogues and recombinant growth factors require specialised biotech manufacturing facilities. OTC products (over-the-counter), i.e. medicines available without a prescription, represent a multi-billion-euro market served by companies such as Bayer Consumer Health, Stada and Klosterfrau. Homeopathic preparations, herbal medicines and dietary supplements form further regulated segments. Digitalisation is increasingly shaping the sector: Digital Health Applications (DiGA) have been reimbursable since 2020, and AI-assisted drug development is significantly shortening time-to-market.
What does a pharmaceutical company do?
Pharmaceutical companies develop, produce and distribute medicines. They cover the entire value chain from research and clinical trials through to market launch and distribution. In Germany, they are supervised by BfArM (the Federal Institute for Drugs and Medical Devices, comparable to the FDA or MHRA).
How are pharmaceutical companies regulated in Germany?
Pharmaceutical companies in Germany must hold a manufacturing authorisation under Section 13 of the AMG (German Medicinal Products Act). All authorised medicines require approval from either BfArM or the European Medicines Agency (EMA). Regular GMP (Good Manufacturing Practice) inspections ensure quality standards are maintained.
Where can I find contact details for pharmaceutical companies in Germany?
Industry associations such as vfa (Association of Research-Based Pharmaceutical Companies) and BPI (Federal Association of the German Pharmaceutical Industry) maintain member directories. Many companies also list their key contacts directly on their websites. Sanoliste provides a searchable directory of pharmaceutical companies in Germany sorted by federal state and city.
How many pharmaceutical companies are there in Germany?
Germany is home to more than 1,000 pharmaceutical companies employing approximately 130,000 people, according to vfa (the Association of Research-Based Pharmaceutical Companies) 2023 data. The sector includes multinational corporations, mid-sized specialty firms, generic manufacturers and biotech startups.
What is BfArM and what does it regulate?
BfArM (Bundesinstitut für Arzneimittel und Medizinprodukte) is Germany's Federal Institute for Drugs and Medical Devices. It is a higher federal authority within the portfolio of the Federal Ministry of Health and is responsible for approving medicines for the German market, monitoring drug safety (pharmacovigilance), regulating narcotics and controlled substances, and overseeing medical devices in Germany. It is broadly comparable to the FDA in the United States or the MHRA in the United Kingdom.
What is the difference between BfArM approval and EMA approval?
Medicines in Germany can be approved through two main routes. BfArM grants national marketing authorisations valid in Germany, or decentralised and mutual recognition procedure approvals valid in multiple EU states. The EMA (European Medicines Agency) grants centralised marketing authorisations valid in all 27 EU member states simultaneously, typically used for innovative biologic medicines, oncology drugs and products for rare diseases.
What does GMP mean in the context of German pharmaceutical manufacturing?
GMP stands for Good Manufacturing Practice. In Germany and the EU, GMP compliance is a legal requirement for all pharmaceutical manufacturers under the AMG and the EU GMP Guidelines (EudraLex Volume 4). GMP covers all aspects of production including premises, equipment, personnel qualification, process validation, documentation and quality control. Compliance is verified by regular inspections from the competent state pharmaceutical supervisory authority.