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Hormosan Pharma GmbH Address & Contact
Hormosan Pharma GmbH at a Glance
The Hormosan Pharma GmbH from Frankfurt am Main is a pharmaceutical company specialized in generics and hormonal preparations in Hesse. With a strong market presence in the German pharmacy market, the company focuses not only on the development but also on the marketing of pharmaceuticals that provide cost-effective alternatives to original products. Particularly in the fields of gynecology and hormone therapy, Hormosan Pharma is active and offers products that meet clinical standards and cater to the needs of doctors and patients.
Services and Products
Hormosan Pharma offers a comprehensive range of hormonal contraceptives, hormone replacement therapies, and other gynecological generics. Among the most well-known products are...
- Hormonal contraceptives: These products provide effective protection against unwanted pregnancies and are available in various dosages and formulations to meet the individual needs of women.
- Hormone replacement therapy: Hormonal substitution therapies support women in the menopausal phase and help relieve symptoms such as hot flashes, sleep disturbances, and depressive moods.
- Generics from other therapy areas: Hormosan Pharma also has a portfolio of general medicine generics used to treat a variety of conditions, from cardiovascular diseases to pain therapies.
All products are approved under German pharmaceutical law and are produced by GMP-certified manufacturers. Hormosan Pharma places great importance on the quality and safety of its medicines and subjects its products to strict controls. The company is established as a reliable generic provider in the German pharmacy market and is appreciated not only by pharmacists but also by doctors who can rely on the effectiveness and tolerability of the preparations.
Regulatory Classification
In Germany, Hormosan Pharma GmbH is subject to stringent regulatory requirements. As a manufacturer of pharmaceuticals, the company must comply with the guidelines of the Medicines Act (AMG). Each product undergoes comprehensive approval processes before market introduction, ensuring the safety, efficacy, and quality of the medicines. Membership in institutions such as the Federal Association of Pharmaceutical Industry (BPI) and the exchange with professional societies underline Hormosan Pharma's responsibility in the pharmaceutical landscape.
Location Frankfurt am Main / Hesse
Frankfurt am Main is a significant location for pharmaceutical companies as a financial and trading center of Europe. The Frankfurt-Rhine-Main metropolitan region provides Hormosan Pharma with excellent infrastructure, a dense network of pharmacy wholesalers, and direct access to international markets. This enables efficient distribution and a quick response to market needs. Furthermore, the company benefits from proximity to top-tier research institutions and universities, fostering collaborations and innovation projects.
Special Features of Hormosan Pharma GmbH
A distinctive feature of Hormosan Pharma is its commitment to sustainability and responsibility. The company pursues an environmentally conscious corporate policy that includes aspects such as reducing its ecological footprint and conserving resources in production. In addition, Hormosan invests in the training and education of its employees to ensure that knowledge and skills are always up to date. Another aspect is the close cooperation with doctors and pharmacists to optimally consider patient needs and support therapeutic decisions.
Other pharmaceutical companies: Overview of Pharmaceutical Companies | Pharmaceutical Companies in Hesse | Pharmaceutical Wholesalers
```Frequently asked questions about Hormosan Pharma GmbH
What does Hormosan Pharma GmbH do?
Hormosan Pharma GmbH stellt innovative Lösungen in the Medikation and Generika her and understützt Heilungserfolge with Aufklärungsmaterialien. Sie specialises in seltene Krankheiten in the Neurologie, wie z.B. the Myotonie or the Myasthenia gravis, on Schmerztherapie, Sexualgesandheit, einschließlich the medizinischen support at HIV-Infektionen.
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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.