-Manage the entire process from drug discovery to clinical trial investigational medicinal product supply.

-Evaluate efficacy of drug candidates through in-vivo and in-vitro testing.

-Enhance pharmaceutical quality through manufacturing process optimization research.

-Carry out synthesis and analytical research to secure reference standards.

-Aim to secure manufacturing process technology through generic drug research.

-Achieve mass production process technology and transfer to GMP production facilities.

-Develop manufacturing processes and conduct labeling studies for domestic production of generic drugs.

-Perform labeling studies for PET (diagnostic) and SPECT (therapeutic) radiopharmaceuticals.

-Establish a labeling center through a network with domestic and international GMP-equipped institutions.

-Develop radiopharmaceuticals using peptides and antibodies.

-Develop theranostic radiopharmaceuticals targeting prostate cancer.

-Research on generic radiopharmaceuticals labeled with Tc-99m for diagnostic purposes.