SRI Biosciences will carry out preclinical testing, good manufacturing practice development, stability studies, human clinical trials and formulation development work for NIAID under the multi-year contract, SRIÂ said Tuesday.
The division will also help the agency move drug candidates through the Food and Drug Administrationâs approval process.
Polly Chang, senior director of molecular and genetic toxicology at SRI Biosciences, said it will leverage its experience in radiation biology research and drug development to support the project.