Events: detail
Understanding US-FDA Drug Submission Procedures
- Hosted by:
- Informa Life Sciences
- Speaker:
- None listed
- Starts:
- September 10, 2007 at 10:15 am
- Ends:
- September 11, 2007 at 06:00 pm
- Location:
- Regus Victoria, Portland House, Stag Place, London, SW1E 5RS United Kingdom
- Maps:
Description
How can you avoid receiving a FDA non-approvable letter? Do you want to be responsible for delaying your drug submission in the USA because you failed to supply the right registration dossier? In the challenging environment of US drug registrations procedures, you need to understand all the current procedures. To help you do this, IPT has developed this course to clarify the US regulatory process. By attending , you will gain a practical insight into FDA’s requirements for new drug development and prepare your new drug registration dossier accordingly to US guidelines.
- Registration required:
- Yes
- Free:
- No
Additional information
Please check conference website for more and the most up-to-date details including the full speaker list and to register online.
For more information
- Contact person:
- IIR PTI Customer Services
- Phone:
- 020 7017 7481
- Email:
- registration [ at ] iir-conferences.com
- Website:
- Understanding US-FDA Drug Submission Procedures
