Events: detail
Adverse Event Reporting and Pharmacovigilance
- Hosted by:
- Informa Life Sciences
- Speaker:
- None listed
- Starts:
- July 16, 2007 at 09:00 am
- Ends:
- July 17, 2007 at 05:00 pm
- Location:
- Regus Victoria, Portland House, , Stag Place, London, SW1E 5RS United Kingdom
- Maps:
Description
Recent times have proved to be the most turbulent in pharmacovigilance for many years. With million dollar fines, tougher guidelines and the introduction of MedDRA, it is crucial that you and your company reduce the risk of incorrect ADR reporting… now. This hands-on course is packed with practical examples and industry case studies to give you the confidence to cope with the daily demands of pharmacovigilance.
- 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 7915 5055
- Email:
- registration [ at ] pti-courses.com
- Website:
- Adverse Event Reporting and Pharmacovigilance
