Numaferm GmbH
Booth number: C28
www.numaferm.com
About us
Born in 2009 at the University in Düsseldorf, Germany, Numaferm became one of the world-leading solution providers for the production of peptides, proteins and pepteins (PEPTides & protEINS, 30-300 aa).
Applying the first biochemical production platform Numaswitch, our team of +30 experts makes the difference to our partners and their development programs. We operate in our 1,000 sqm facilitiy with state-of-the-art infrastructure and equipment under a strict quality management system (ISO9001:2015), meeting highest market standards.
Numaferm accelerates, increases safety profiles and develops stand-alone production processes, outperforming next best alternatives. We have demonstrated our advantages in more than 200 successful projects globally for over 50 partners, covering Big Pharma, Biotech and world-leading Life Science organizations.
Our mission is to support you, independently of your target - in time, at cost, scale and quality, in a sustainable way and trustful relation.
Address
Merowingerplatz 1a
40225 Duesseldorf
Germany
Phone: +49 2119 7532900
Merowingerplatz 1a
40225 Duesseldorf
Germany
E-mail: info@numaferm.com
Phone: +49 2119 7532900
Internet: www.numaferm.com
Contact person:
Dr. Christian Schwarz
CEO
E-mail: christian.schwarz@numaferm.com
Phone: +49 1608 385834
Products & Services
By applying the biochemical production platform and standardized work streams, we can offer the release of cGMP peptides and proteins within 9 months.
As part of the first development program, a cell line, as well as a mg sample is prepared within 1 month. Following this, the process development program (~ two months) results in g scale processes, suitable for tech-transfers into GMP environments.
The process is applied to produce up to 100 g GLP-material for toxicity and animal studies. For GMP production, process descriptions and analytics are converted into SOPs, cells and additional material is generated and the best production partner is chosen from our vast network of established GMP-conform CDMO partners.
With a high degree of standardization and parallelizing necessary work packages, we set new standards in the protein world, accelerate your developments, and bring needed treatments to patients in-time and at highest quality.
