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Omega Pharma GmbH Address & Contact
Company profile
1987
Founded
9.000+ (global, Perrigo)
Employees
Omega Pharma GmbH Overview
Omega Pharma GmbH is the German subsidiary of the Belgian OTC pharmaceutical group Omega Pharma, which has been a part of Perrigo Company plc since 2015. The German subsidiary is based in Böblingen, Baden-Württemberg. Omega Pharma GmbH specializes in the development, production, and marketing of over-the-counter pharmaceutical products that play an important role in self-medication and health management. The company focuses on providing innovative solutions that meet the health needs of consumers and works closely on improving people's quality of life.
OTC Health Products and Self-Medication
Omega Pharma is represented in Germany with a versatile range of over-the-counter health products. Well-known brands include Wartner (wart removal), Solgar (nutritional supplements), Excilor (nail fungus treatment), ACO (skin care), and Fytocare (herbal products). The company's commitment to self-medication is particularly noteworthy, as Omega Pharma's products not only relieve discomfort but also promote a healthy lifestyle. The over-the-counter products are formulated to impress with their efficacy and safety and contribute to the alleviation of healthcare burdens. In addition, the company meets the stringent requirements of the European Medicines Agency (EMA) as well as local regulatory authorities responsible for product quality.
Regulatory Classification and Quality Standards
The products of Omega Pharma are manufactured and distributed in accordance with European regulations for medicines and dietary supplements. This means that they are subject to the highest quality standards and the strict requirements of Good Manufacturing Practice (GMP). Furthermore, the products are continuously tested for safety and efficacy to best protect the health of consumers. Omega Pharma places great importance on comprehensive clinical studies and market analyses to accurately capture consumer needs and develop innovative, evidence-based products.
Location Böblingen
Böblingen in Baden-Württemberg is the administrative headquarters of the German Omega Pharma subsidiary. From here, pharmacies and drugstores in Germany are supplied with OTC branded products, and the sales team for the pharmacy market is coordinated. The location in Böblingen also offers excellent conditions for research and development, as it is situated in one of Germany's strongest economic regions, known for its innovation. This enables close cooperation with universities and research institutes on-site to develop new products and optimize existing formulations.
Regional Significance and Social Responsibility
Omega Pharma plays a significant role in the Böblingen region, both as an employer and as a company committed to social responsibility. By creating jobs, the company contributes to the economic stability of the region. Furthermore, Omega Pharma promotes various health initiatives and educational programs to strengthen health awareness in the population. The company actively participates in local events and supports health campaigns that promote awareness of self-determined health decisions.
Special Features and Innovations
A unique feature of Omega Pharma is its focus on herbal products and natural remedies, which is reflected in the Fytocare product line. Here, the company combines tradition with innovation, offering solutions based on herbal ingredients. Through intensive research in this area, Omega Pharma is able to provide products that are both effective and well-tolerated. The company also remains at the forefront of modernity and integrates modern technologies into product development, further increasing the efficiency and effectiveness of the products. Innovative marketing approaches and digital strategies ensure that Omega Pharma's products reach end consumers more easily and specifically.
More pharmaceutical companies in Germany | pharmaceutical companies in Böblingen | pharmaceutical companies in Baden-Württemberg
Frequently asked questions about Omega Pharma GmbH
What does Omega Pharma GmbH do?
Omega Pharma Deutschland GmbH stellt rezeptfreie medicines, Körperpflegeprodukte and Nahrungsergänzungswithtel her and vermarktet sie. Zu ihrer Produktpalette gehören u.a. Mittel zur Gewichtsreduzierung, gegen urologische Leiden, at Augenleiden or Hautproblemen, wie z.B. Warzen, Tests, um eine Schwangerschaft festzustellen and Insektenschutz.
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Pharmaceutical Companies in Germany
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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.