DMF Update
FDA has accepted Andelyn's GMP plasmid DNA drug master file (DMF), which enables the organization to vertically integrate its clients' manufacturing process, condensing timelines for developers to begin manufacturing to just three months.
FDA has accepted Andelyn's GMP plasmid DNA drug master file (DMF), which enables the organization to vertically integrate its clients' manufacturing process, condensing timelines for developers to begin manufacturing to just three months.