AGC Biologics to build new facility in Japan
The facility, which is part of the company’s strategic growth plan, aims to enhance pharmaceutical development and manufacturing offerings in Asia. This will aid in meeting the increasing
The US Food and Drug Administration (FDA) has granted priority review to Roche’s supplemental biologics licence application (sBLA) for Gazyva/Gazyvaro (obinutuzumab) to treat adults with primary membranous nephropathy (pMN).
This partnership covers drug-linker technology and CRDMO services right from discovery to commercialisation. WuXi XDC CEO Dr. Jimmy Li said, “IntoCell’s unique drug-linker technologies and our leading, open-access