12/03/2026
We’re thrilled to share that the U.S. FDA has officially accepted the DMF for our PSMA-I&T.
This is an important milestone for us and highlights our capabilities in product development, quality management, and global regulatory compliance.
Our GMP-registered products—including Mannose triflate, PSMA11, MDP, DOTA-TATE ACETATE, and R-PSMA I&T—are ready to support regulatory.
We’re always open to LOA requests and collaboration opportunities. Let’s work together to advance precision nuclear medicine!