You need a CDMO with the competency, skills and regulatory knowledge to develop and manufacture your product. Oncowitan can help you to select the best CDMO, adapted to your project and timelines: Drug Substance (DS) and/or Drug Product (DP); capacities; technologies and equipment; safety, containment; regulatory compliance (EU, US); location…
Support your business expansion, review market opportunities, working closely with your teams to foster innovation in new products, processes and services.
Good knowledge of the CDMO environment in Europe, in particular for Oncology products
- Injectables cytotoxics
- Targeted therapeutics
- Biotech products (mAbs and ADC)