active ingredients and pharmaceuticals to the highest international standards.
Since 2008, we have been a subsidiary of
FAREVA Group, which operates in 13 countries and has 41 production sites and 16 research and development centers around the world.
Our key focus is on developing and manufacturing products for cancer treatment and immunosuppressive therapies.
Finished Dosage Forms
Developing and manufacturing products from tablets and capsules up to final packaging.
We are specialized in high containment solutions. Our experience includes:
- High containment up to OEB 6
- DoE, QbD, PAT
- Clinical phases II and III
- Commercial production for more than 100 countries
Both drug substance and drug product activities are located at one site spanning almost 60,000 m2 in Feucht, near Nuremberg, Germany
Pharmaceutical ingredients
Developing and manufacturing highly potent APIs at level OEB 4 to OEB 6
- Over 100 organic reactions
- Syntheses with up to 12 steps
- From clinical phase II all the way to market approval
- 250 l and 800 l reactors
- Large scale manufacturing 4.000 l up to OEB 4
- Production quantities: 5 kg to 20 tons
We don’t just work
for the Big Five.
We work with big pharma, medium-sized companies, start-ups and virtual companies. Our goal is to build long-term partnerships with our customers and suppliers.
Norbert Straub, R&D Director Pharma Highly Potent
Norbert Straub, R&D Director Pharma Highly Potent
Dr. Angrit Trapp, Director Customer Relations
We are purely a contract manufacturer and do not develop brands of our own
We are your partner, not your competitor.
Dr. Angrit Trapp, Director Customer Relations
One Stop Shop:
From active ingredient synthesis
to the finished product
We offer complete development
– including scale-up and one-to-one transfer of the manufacturing process –
all the way through to commercial manufacturing.
This is by no means standard for a company of our size.
But we have what it takes: Our employees are extremely well trained,
our analytics department is perfectly equipped and our facilities are
versatile to handle both clinical and commercial programs.
Apart from our services, we also offer a portfolio
of around 30 active ingredients for the generics market.
Dr. Georg Straller, Head of Development and Transfer, Pharma
Clients can expect transparency and collaboration at every stage of the process.
We strive to meet our customer’s expectations.
Dr. Georg Straller, Abteilungsleiter Entwicklung und Transfer, Pharma
We are regularly inspected by foreign health authorities.
We offer extensive support for global regulatory approvals of active pharmaceutical ingredients.
Dr. Christine Sonner, Director Quality Management
Dr. Christine Sonner, Director Quality Management
Nils Wendland, Regulatory Affairs
We have decades of experience with various health authorities.
We offer extensive support for global regulatory approvals of active pharmaceutical ingredients.
Nils Wendland, Regulatory Affairs
Excerpt from our audit history
• Germany: Government of Upper Franconia, last inspection: May 2018, pharmaceutical ingredients May 2022
• USA: FDA, last inspection: July 2019
• Russia: State Institute of Drugs and Good Practices, last inspection: February 2022
• Brazil: ANVISA, last inspection: June 2018
• Korea: Ministry of Food and Drug Safety, last inspection: 2016
• Turkey: last inspection 2018
We support clients
in over 100 countries
We have clients in USA, Japan, Europe, Russia,
Korea, China, Brazil, Australia, New Zealand, Taiwan, Africa…
We adapt to the most diverse mentalities – and enjoy it.
Occupational safety, environmental protection, and process safety are extremely important to us.
Employee safety is our top priority. Always and without exception. Additionally, environmental protection is fundamental focus area for the site. For example, we base our work on HAZOP.
We can work with very low OELs, down to 10 ng/m3.
Our employees are well trained and our facilities are fully equipped – from sophisticated building automation to dust extractors, waste air scrubbers and much more.
Daniela Kovats, Manager EHS
Daniela Kovats, Manager EHS
Most of our employees have worked for us for many years, some for several decades.
Our team is made up of chemical technicians, chemical laboratory assistants, pharmaceutical technicians, pharmacists, chemists and chemical engineers. We have extensive expertise and a wealth of experience in process and analytical development and manufacturing.
This experience allows us to make valuable recommendations during the project and to get results quickly.
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ABOUT US
We deliver the complete process from development through production to packaging of your medicines.