Services
Your product development process requires both experience and expertise. We offer you a customized development package, based on your needs and the regulatory phase and in compliance with cGMP/ISO13485. As a well-experienced Contract Development and Manufacturing Organization (CDMO), we will help you overcome potential development challenges, thus saving you time and avoiding unnecessary expenses, from drug development and all the way to clinical trials manufacturing.
Read more about our services below or contact us.
Manufacturing
R&D and GMP/ISO13485 production of semi-solids, and liquids, and for both aseptic and non-aseptic products.
Manufacturing
Analytics
Full analytical package for product characterization: method development and validation, product release and shelf life, and QC testing.
Analytics
Chemistry
Development of economically efficient and proprietary processes for new drug candidates and lead compounds.