European Production Facilities
Highest International Standard
Daiichi Sankyo Europe has two production facilities, both approved by national and international authorities such as the U.S. Food and Drug Administration (FDA), the European Medicines Agency (EMA) or the German Institute for Drugs and Medical Devices (Bundesinstitut für Arzneimittel und Medizinprodukte or BfArM). Our manufacturing facilities comply with GMP (Good Manufacturing Practices) standards.
State-of-the-art equipment and automation using the latest technology ensure consistently high production quality. In the company's global pharmaceutical production operations, the role of the Pfaffenhofen production plant continues to expand.
The site makes an important contribution to global production capacity. The whole family of Daiichi Sankyo olmesartan products is produced in Pfaffenhofen and shipped from this location.
Pfaffenhofen: Pharmaceutical Goods Worldwide
More than 28 million packages and approximately 2 billion tablets of our products can be produced each year at our site located in the German state of Bavaria. From here, they are shipped throughout the world. In co-operation with licensees, we distribute pharmaceutical goods to more than 50 countries worldwide, including toll manufacturing for the U.S. and Asian markets. Pfaffenhofen's activities comprise biotechnology manufacturing and the production of semisolid, liquid (ointments, gels) and solid (tablets and film-coated tablets) pharmaceutical products.
In our production facility in Altkirch, France, we manufacture active pharmaceutical ingredients for our traditional Luitpold products.
The Pfaffenhofen site plays a key role in pharmaceutical development and assumes a leading role globally for an increasingly large number of galenic research projects. In the pharmaceutical development department in Pfaffenhofen, more than 70 employees work on development projects for Daiichi Sankyo worldwide.
The department is integrated into Daiichi Sankyo’s global research structure and reports directly to the Group’s Global Head of Research.
The German team investigates how active ingredients are metabolised, defines the optimal formulation for the related medicine, examines the best production methods for the drug and evaluates the stability of the new drug formulation.