Active pharmaceutical ingredients and CDMO

GMP API & CDMO Made in Germany

Your active ingredient partner from Germany

Since the start of active ingredient production at our site in 1874, we have consistently focused on reliability and the highest quality “Made in Germany.”

Today, Arevipharma is a cGMP pharmaceutical manufacturer with a strong focus on narcotics. We offer our global customers both our own products and CDMO projects. We look forward to receiving your inquiries!

Flexibility

We are a privately owned, medium-sized company that stands for agility, flexibility, and absolute reliability, with short decision-making processes. At our facility, we manufacture cGMP APIs in quantities ranging from a few grams to several metric tons.

Sense of Responsibility

With our active ingredients, we make a significant contribution to the health of millions of people around the world and hold ourselves to the highest standards of quality in our products and our operations.

Experience

Our teams of project managers, process chemists, process engineers, and colleagues from the quality and regulatory departments guarantee first-class customer service and decades of experience in the synthesis of drug substances.

Consulting Expertise

We serve customers in all major global pharmaceutical markets and, as a result, offer comprehensive expertise in all technical and regulatory requirements our partners face when seeking global approvals.

Safety

The protection of our employees, the environment and the safety of our production facilities is our top priority. As a German manufacturer, we ensure the highest cGMP and HSE standards for our partners.

Your Trusted Partner for cGMP Active Pharmaceutical Ingredients

From grams to tons

Arevipharma is a medium-sized manufacturer of active pharmaceutical ingredients and contract manufacturer for pharmaceutical customers around the world. In our production facilities in Radebeul, we develop, produce and store APIs of numerous volume and safety classes, specialising in the complex and demanding handling of narcotics.
Our more than 150-year company history as a manufacturing site for synthetic active ingredients is the DNA of our value creation. As a fully integrated location, we have the ability to react quickly, flexibly, comprehensively, sustainably and reliably to the enquiries and requirements of our global customers and business partners.

Development

Experienced chemists and project managers develop and optimise synthesis processes to the latest scientific standards, tailor-made for our production facilities

Production

We have five production facilities for the cGMP manufacture of all API volumes in the range of a few grams to many tonnes

Logistics

Numerous storage options for many temperature ranges and substance classes are available at the Radebeul site.

Quality Control

We develop, validate, and implement all necessary analytical methods. As part of our daily routine, we ensure that all raw materials, intermediates, and finished products are tested against their respective specifications.

Quality Assurance

We are committed to our quality policy. Our management is committed to strict compliance with all cGMP requirements. We ensure that all processes are carried out in accordance with regulatory requirements and the needs of our customers.

Regulatory Affairs

We hold over 150 authorisations for our active substances and are represented with them on all continents and in the largest global pharmaceutical markets.

Sales

A team of sales people, project managers, sales operations and supply chain specialists serve global small, medium and big pharma customers to underline our outstanding quality with the best customer service.

Active pharmaceutical ingredients since 1874

Our history

Arevipharma’s roots date back to 1874. The “Salicylic Acid Factory Dr. F. von Heyden” produced the world’s first active ingredient manufactured by a technical process.