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:
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.