09. - 10.06.2008

Prague: The FDA Organisation, Inspection, Application and Approval

During this two days seminar in Prague, the attendees learnt from Dr. Hiltrud Horn the essentials about regulatory requirements in US and preparation of dossiers in US. Furthermore Dr. Horn presented case studies about the important aspects during drug development.

(Conference organized by Concept Heidelberg)



Back

HOTLINE

Phone +49 (0) 7251/305 529
Fax +49 (0) 7251/305 528
Mail

Events

  • 18.-19.06.2024
    Online Seminar: Der Regulatory Affairs Manager
    More
Get all events



News

  • 19.12.2022
    EU Update regarding Deadlines of Nitrosamine Impurities
    More
  • 01.09.2022
    EU-GMP Annex 1 finally published
    More
  • 26.08.2022
    New Deadlines and Chances for Nitrosamines
    More
Get all news