ViiV Healthcare GmbH
Pharmaceutical Companies · München
ViiV Healthcare GmbH is the German subsidiary of auf HIV-Therapien spezialisierten Unternehmens ViiV Healthcare, based in München.
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ViiV Healthcare GmbH Address & Contact
Company profile
2009
Founded
ViiV Healthcare GmbH Overview
ViiV Healthcare GmbH is the German subsidiary of ViiV Healthcare Limited, a pharmaceutical company specializing in HIV therapeutics, which was founded in 2009 as a joint venture between GlaxoSmithKline (GSK) and Pfizer. In 2012, Shionogi & Co. joined as a third partner. ViiV Healthcare focuses exclusively on HIV and AIDS and is considered one of the most innovative companies in this field worldwide. The German subsidiary in Munich coordinates the German HIV medicine market, served by a specialized network of HIV-focused practices, outpatient clinics, and hospitals. Additionally, the Munich headquarters plays a key role in European product development and strategy, highlighting the company's regional significance.
Field of Activity & Products
ViiV Healthcare has developed and marketed several significant HIV therapeutics that are used globally. Key products include Triumeq (Abacavir/Lamivudine/Dolutegravir) and Tivicay (Dolutegravir), two integrase inhibitors that are part of standard therapies in HIV treatment. Cabenuva (Cabotegravir/Rilpivirine), a monthly or bi-monthly injectable HIV regimen, is a groundbreaking product that enables non-daily HIV therapy for the first time. Apretude (Cabotegravir) is an injection solution for HIV pre-exposure prophylaxis (PrEP). Furthermore, ViiV Healthcare also provides support in the form of clinical trials and educational programs to ensure that healthcare professionals and patients are well-informed. ViiV Healthcare is also committed to global initiatives to combat the HIV epidemic in low-income countries, working closely with local organizations and governments.
Research & Regulation
ViiV Healthcare invests heavily in clinical research for new HIV therapeutic approaches, including long-acting regimens and cure strategies. The company has made significant advancements in drug development, safety, and efficacy, as demonstrated by numerous clinical trials. All products sold in Germany are regulated by the Federal Institute for Drugs and Medical Devices (BfArM) and the European Medicines Agency (EMA). ViiV Healthcare is a member of the Association of Research-Based Pharmaceutical Companies (vfa) and actively advocates for transparency and adherence to high ethical standards in drug development. The close collaboration with experts from clinical and academic fields enables ViiV Healthcare to remain at the forefront of medical research.
Sustainability and Social Responsibility
ViiV Healthcare not only pursues economic goals but also places great importance on sustainability and social responsibility. As part of its social responsibility programs, the company is engaged in raising awareness about HIV and AIDS to reduce stigma and facilitate access to treatment options. This includes collaboration with organizations that care for vulnerable populations as well as promoting educational opportunities in healthcare. In Germany, ViiV Healthcare regularly conducts events and workshops to inform professionals and affected individuals about the latest developments in HIV research and treatment.
Regional Significance & Future Perspectives
As one of the leading providers of HIV-related therapeutics, ViiV Healthcare has taken on a pivotal role in the German and European pharmaceutical supply. The Munich subsidiary not only serves as an important hub for distribution but also for the development of new products specifically tailored to the needs of the European market. The company plans to continue investing significantly in research and development to address the ever-growing challenge of the HIV epidemic. Innovative approaches, particularly in the area of prevention and treatment, are central to the company's strategy.
More information: Pharmaceutical companies in Bavaria or all pharmaceutical companies in Germany on Sanoliste.
Frequently asked questions about ViiV Healthcare GmbH
What does ViiV Healthcare GmbH do?
ViiV Healthcare GmbH is a pharmaceutical company based in München that develops, manufactures or distributes pharmaceutical products. The company is active in the German healthcare market.
Where is ViiV Healthcare GmbH located?
ViiV Healthcare GmbH is headquartered in München, Germany. More information can be found on the company's website.
What products does ViiV Healthcare GmbH distribute?
ViiV Healthcare 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.
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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.