medac | medac CDMO

Our services

Partner with us for trusted, flexible CDMO solutions - from early development to full-scale commercial supply. We're here to bring your innovation to market, safely and swiftly. Explore our Services and Technological Capabilities to find out more.

Commercial

Efficient large-scale bulk manufacturing to support long-term, stable supply

Clinical

Flexible GMP bulk manufacturing for early-phase products with seamless scale-up to commercial production

Molecule types

Small Molecules, Biologics (e.g. mAs, proteins, peptides), Oligonucleotides, Antibody-Drug Conjugates (ADCs)

Dosage forms

Pre-filled syringes, Vials, Cartridges

Process capabilities

Aseptic filling, Terminal sterilisation, Lyophilisation, High potent API (down to OEL = 10 ng/m3), Organic solvent handling

Manufacturing scale

Small scale: 1 – 50 L, Large scale: 50 – 1,500 L, Campaigns: up to 11,000 L

Why choose medac CDMO as your preferred partner?

At medac, we do not just respond to challenges — we anticipate them. Our unwavering commitment to foresight, progress, reliability and creative solution thinking makes us a solution ahead. Our open, responsive collaboration adapts to your goals, creating a partnership built on trust and transparency.

In the dynamic pharmaceutical industry, we understand that staying ahead means more than just keeping pace — it means proactively shaping the future. Therefore, we incorporate forward-thinking into every stage of our process, from early development through commercial production. With two dedicated European production sites, our clients benefit from solutions that are not only for today’s needs but designed to meet tomorrow’s demands as well.

We are prepared to respond flexibly to our clients’ needs whether navigating complex regulatory landscapes, optimising production efficiency or scaling seamlessly from clinical to commercial manufacturing. Our proactive mindset means that we address potential obstacles before they arise. Through our strong focus on quality, compliance and speed, we provide our partners with peace of mind and a competitive edge for global markets.

With medac CDMO, you are choosing a partner who is a solution ahead.

Quality – proven by international health authorities

At medac, quality is not just a requirement - it's the foundation of everything we do. Our quality system is led by experienced professionals and embedded in our daily operations. It ensures that all products and processes meet the highest standards - reliably and consistently.

With more than 40 years of regulatory expertise, we continuously develop our quality system in line with evolving global requirements. It is fully compliant with EU GMP, ICH, WHO, PIC/S guidelines— and regularly audited and approved by international health authorities, including:

European Authorities
US FDA
ANVISA Brazil
PMDA Japan
Health Canada
MFDS South Korea
Russian Authorities
Saudi Arabia Authority
Kazakhstan Authority
Iraqi Authority
Libyan Authority

Our locations

Our three European sites deliver tailored sterile manufacturing solutions: Wedel (Headquarters, Germany), Dessau (Germany) and Brno (Czech Republic).

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News & Events

28.03.2025

CDMO medac Group Celebrates the Launch of the next Production Line

medac Group, a trusted partner in contract development and manufacturing, proudly announces the successful commissioning of its latest investment: the third production line at oncomed, a state-of-the-art production site in the Czech Republic.

Find out more

CDMO medac Group Celebrates the Launch of the next Production Line

BIO International Convention 2025 (16.06. - 19.06.2025)

The global stage for biotech – BIO International Convention 2025 brings together the world’s most influential biotech and pharma players. Whether you're developing cutting-edge biologics or looking for a reliable CDMO partner, let’s explore how we can work together.