Pharmcann Deutschland AG
Pharmaceutical Companies · München
Pharmcann Deutschland AG is a pharmaceutical company based in München, Bavaria, 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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Pharmcann Deutschland AG Address & Contact
Pharmcann Deutschland AG Overview
Pharmcann Deutschland AG is a pharmaceutical company based in Munich, operating in the field of medical cannabis. The company is part of the growing segment of cannabis-based therapies in Germany and operates within the legal regulations of the German Narcotics Act (BtMG). Since its inception, Pharmcann has positioned itself as an innovative player that supports patients with high-quality cannabis products and bridges the gap between tradition and modernity in therapy research.
Field of Activity & Products
Pharmcann Deutschland AG is involved in the procurement, quality assurance, and distribution of medical cannabis products. The company targets specialists, pharmacies, and pharmaceutical wholesalers in Germany. Medical cannabis has been prescribable to patients with certain conditions since 2017 – including chronic pain, multiple sclerosis, and loss of appetite in severe illnesses – and can be reimbursed by health insurance.
- Product Areas:
- Flowers: High-quality cannabis flowers available in various strains to meet different therapeutic needs.
- Oils: Extracts in the form of oils that allow for precise dosing and versatile applications.
- Capsules: Ready-made capsules that provide ease of intake and better dosage accuracy.
The product portfolio of Pharmcann includes both THC-containing and CBD-containing products, allowing for a differentiated approach to various indications. The company collaborates closely with research institutions to further develop application possibilities and improve patient care. The activities aim to offer patients a safe, effective, and high-quality form of therapy.
Regulation
As a cannabis company, Pharmcann Deutschland AG is subject to the stringent requirements of the BfArM and the Cannabis Agency. The company is organized as a joint-stock corporation (AG) and is therefore committed to particularly transparent corporate governance. The activities are subject to the control regulations of the BtMG as well as the BtMVV (Narcotics Prescription Regulation). These regulations guarantee the safety and efficiency of the products, especially in a field heavily influenced by regulatory frameworks.
A central challenge for Pharmcann is the continuous adaptation to changing legal requirements regarding the cultivation, processing, and distribution of cannabis products. The company has implemented comprehensive compliance management systems to meet the high demands of the market at all times. The transparent communication of corporate activities also contributes to the education about medical cannabis.
Regional Importance
As a company based in Munich, Pharmcann Deutschland AG contributes to regional economic development. By creating jobs and collaborating with local partners in research and education, the company is firmly rooted in the Bavarian capital. This locational advantage enables Pharmcann to respond quickly to local market needs while also connecting to supraregional developments. Additionally, being located in one of Germany's most significant health locations guarantees access to a network of specialized facilities and experts.
Particular Features
A notable aspect of Pharmcann Deutschland AG is its commitment to quality and sustainability. The company pursues a sustainable cultivation method based on ecological practices to minimize environmental impact. Furthermore, Pharmcann invests in the training of professionals in the handling of medical cannabis, thereby contributing to the establishment of expertise in the healthcare sector.
Additionally, Pharmcann is engaged in educating doctors and patients about medical cannabis to reduce prejudices and enhance understanding of the therapy form. The goal is to increase acceptance and professional knowledge about the application possibilities of cannabis in therapy.
More information: Pharmaceutical companies in Bavaria or all pharmaceutical companies in Germany on Sanoliste.
Frequently asked questions about Pharmcann Deutschland AG
What does Pharmcann Deutschland AG do?
Pharmcann Deutschland AG gehört zu einer panEuropean companysgruppe, the sich with Anbau and distribution of medizinischen Cannabisprodukten beschäftigt. Im German Zweigundernehmen geht es um den Import, um Freigabe and distribution the medizinischen products.
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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.