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$150
Learn the FDA-required testing and safety assessments needed to for a successful IND.
$150
Learn the workflow and CMC considerations for manufacturing AAV gene therapy products.
$150
Learn which studies are undertaken, their purpose, and the common endpoints of a successful Phase I ...
$150
Learn the purpose, trial designs, and the FDA and EMA special designations for Phase II and III cli...
$150
Learn the ongoing post-approval clinical assessments required by regulatory agencies.
$150
Learn the four fundamental business aspects of biopharma, including financing, IP law, life cycle ma...
$150
Learn the foundational science and the regulatory approval process for gene therapy.