Galderma Laboratorium GmbH

Pharmaceutical Companies · Düsseldorf

Galderma Laboratorium GmbH is the German subsidiary of auf Dermatologie spezialisierten Unternehmens Galderma, based in Düsseldorf.

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Galderma Laboratorium GmbH Address & Contact

Address

Toulouser Allee 23a
40211 Düsseldorf

Company profile

1981

Founded

5.000+

Employees

Galderma Laboratorium GmbH Overview

Galderma Laboratorium GmbH is the German branch of Galderma, the world's largest pure dermatology company. Founded in 1981 as a joint venture between Nestlé and L'Oréal, Galderma has since evolved into an independent market leader in medical and aesthetic dermatology. The German branch is located in Düsseldorf and plays a central role in the company structure, as it connects to a large network of dermatologists, specialists, and decision-makers in the German healthcare system.

The core values of Galderma are based on scientific excellence, customer orientation, and innovation. These values are reflected not only in product development but also in the continuous training programs that support medical professionals in Germany.

Medical and Aesthetic Dermatology

Galderma offers a comprehensive product portfolio that includes both prescription medications and aesthetic solutions. Therapeutic areas include products for the treatment of:

  • Acne: Differin and Epiduo are proven products used to improve acne symptoms.
  • Rosacea: Soolantra and Mirvaso provide effective options for controlling this common skin condition.
  • Psoriasis and Eczema: Therapeutics aimed at alleviating symptoms and improving the quality of life for those affected.

In dermatologic oncology, Galderma employs modern approaches for the treatment of skin cancers, particularly basal cell carcinoma and actinic keratosis. Innovative active ingredients are used that target cancer cells directly, thereby reducing the need for invasive interventions.

The aesthetic segment is covered by high-quality fillers, primarily based on hyaluronic acid. Brands like Restylane and Sculptra have made a name for themselves internationally and are well established in aesthetic medicine. These products are used not only in clinics but also by dermatological practices to improve the appearance of the skin and restore youthful freshness.

An important component of the portfolio is the consumer brand Cetaphil, which is globally appreciated for its skin-friendliness and mild formulations, particularly by users with sensitive skin. Cetaphil products are available in pharmacies as well as retail stores, significantly enhancing Galderma's reach and influence in the skincare sector.

Regulatory Classification and Quality Assurance

Galderma is subject to strict regulatory frameworks that are relevant for pharmaceutical companies in Germany and the EU. All products undergo extensive clinical trials and must meet the requirements of the European Medicines Agency (EMA). Quality assurance and compliance are therefore fundamental aspects of the company's philosophy. Galderma continuously invests in research and development to ensure that products are not only effective but also meet the latest safety standards.

Location Düsseldorf

Düsseldorf is strategically advantageous for Galderma's activities in Germany. The city has established itself as a center for pharmaceuticals and medical technology, hosting numerous specialists and clinics. As the headquarters of the German Galderma branch, it enables maintaining relationships with dermatologists and aesthetic medical professionals across the country. The annual DDG conference, one of the largest dermatology events in Germany, provides a platform for showcasing new products and promoting knowledge exchange among professionals. These events are critical for positioning Galderma as a thought leader in dermatology.

In addition, Galderma is involved in various social initiatives to raise awareness of dermatological diseases and provide education. The company sees it as its responsibility to engage in society and highlight the concerns of patients.

More Pharmaceutical companies in Germany | Pharmaceutical companies in Düsseldorf | Pharmaceutical companies in NRW

Frequently asked questions about Galderma Laboratorium GmbH

What does Galderma Laboratorium GmbH do?

Galderma Laboratorium GmbH is a pharmaceutical company based in Düsseldorf that develops, manufactures or distributes pharmaceutical products. The company is active in the German healthcare market.

Where is Galderma Laboratorium GmbH located?

Galderma Laboratorium GmbH is headquartered in Düsseldorf, Germany. More information can be found on the company's website.

What products does Galderma Laboratorium GmbH distribute?

Galderma Laboratorium 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.

Galderma Laboratorium 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.

Last updated: 17.04.2026 · Category: Pharmaceutical Companies