The FDA’s May 2026 guidance on cell and gene therapies provides for CMC flexibilities while insisting on quality and ...
A key theme emerging from FDA complete response letters since 2018 is that data system validation is lacking in the ...
Earlier this week, contract development and manufacturing organization (CDMO) Cellares announced its partnership with ...
BioProcess International learned about how advanced therapy developers and manufacturers are adapting to changing ...
BPI Contributor Sidharth Ananthanarayan ...