Annual Report

[FDA] post-approval studies (PAS), which are submitted after the NDA has been approved but before marketing authorization, provide additional information about the safety and effectiveness of the product. They may include clinical trials conducted after the initial approval, and they may update previous information. PAS are typically published electronically.

More information about Annual Report

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Mablink
Gustave Roussy
Beyond Spring
Clinical Services
NS Pharma
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