A RELIABLE PARTNER – WE MAKE CELL THERAPY WORK FOR YOU!


“We are ready to support you on your way to the clinic from any stage in product development. Whether you are still growing your cells in small cell culture flasks in a university lab, or you already have the GMP process established, we can develop and transfer your process into the GMP-compliant production of a clinic-ready Investigational Medicinal Product.”

Ulrike Verzetnitsch, CTO

apceth Biopharma ‘s comprehensive GMP services offer:
  • Highest GMP- and quality standards in ATMP manufacturing.
  • Unique state-of-the-art cleanroom facilities with GMP and BSL2 certification, authorizing work with genetically engineered cells and viral vector systems.
  • Dynamic, committed team of experienced senior scientists and technicians.
  • Central location in Europe enabling fast supply of IMPs across the continent.
  • Proven track record of successful industrial collaborations with partners from big pharma, biotech and academia.

Our goal is to be a valuable asset for your business and your product.
With this in mind, apceth Biopharma places great emphasis on:


SERVICE EXCELLENCE

We are a trusted, committed, high-performance partner for our clients, with the highest sense of responsibility and professional integrity.

THINKING OUTSIDE THE BOX

Being ready to take new paths and implement fresh ideas enables us to design and deliver the best solutions tailor-made for the specific needs of every product, every client and every stage of pharmaceutical development.

SYNERGY OF GMP STANDARDS & SCIENTIFIC KNOWLEDGE

We successfully combine the highest GMP standards and state-of-the-art technologies with innovative ideas and scientific know-how. We are proud to offer an optimal balance of GMP experience and comprehensive scientific knowledge.

PERPETUAL & DYNAMIC INTERACTION WITH OUR CLIENTS

Continuous communication is the key to meeting all the needs of our clients, move fast and to react promptly to changing circumstances. Designing our clients’ products is a joint effort: we think, talk and work together closely, we share our clients’ enthusiasm and we assist them in turning their ideas and projects into successful reality.

RISK BASED APPROACH

We prioritize risk management and work hard to identify, assess and remove all potential hurdles in the project and to ensure efficient, timely and straightforward achievement of our clients’ goals.

CLOSE COLLABORATION WITH
REGULATORY AUTHORITIES

We work together with regulatory agencies at all stages of the process and product development. Our clients are assured full regulatory compliance for all developmental activities as well as for final products and processes.

BEING ALWAYS STATE-OF-THE-ART

Through continuous improvement, ongoing learning and development, we are able to satisfy even the most demanding scientific, technological and regulatory requirements relating to our clients’ products in the rapidly evolving ATMP field.

BEING RIGHT IN THE MIDDLE, NOT ON THE SIDELINES

We are one of the major players in the European ATMP sector. We keep close contact with the regulatory agencies and leading scientists in relevant fields. We actively participate in leading discussions and developments in our special areas, contributing to shaping the future of the global ATMP market.

LIVELY AND PRODUCTIVE TEAMWORK

Our highly motivated multidisciplinary team of biologists, pharmacists, engineers, medical professionals and technicians takes responsibility for our clients’ individual needs and meets them in the best possible way.