メニュー 戻るAgenda

Regulatory Affairs: The IND, NDA, and Post-Marketing

Attend this virtual training course to learn about FDA regulations and expectations for the content, submission and review of INDs/NDAs, and the importance of regulatory strategy.


アジェンダ

関連イベント

  • Online

    Drug Development and Lifecycle Management eLearning Program

    Learn how organizations structure their efforts and utilize their resources to improve the odds of successful development in this six module program.

  • 対面受講

    Navigating Chemistry, Manufacturing, and Controls Through the Drug Development Process

    This interactive virtual training course will demonstrate CMC sections of regulatory submissions, the FDA inspection process, and how to avoid or minimize 483s (noncompliance) using real-life scenarios.

  • 対面受講

    Regulatory Affairs: The IND, NDA, and Post-Marketing

    Attend this virtual training course to learn about FDA regulations and expectations for the content, submission and review of INDs/NDAs, and the importance of regulatory strategy.

  • 対面受講

    Regulatory Affairs: The IND, NDA, and Post-Marketing

    Attend this virtual training course to learn about FDA regulations and expectations for the content, submission and review of INDs/NDAs, and the importance of regulatory strategy.

お問い合わせ

Registration Questions?

Send Email
1.888.257.6457
+1.215.442.6100


Agenda and Event Logistics

Send Email
+1.215.442.6108