 Event
detail
|
| Dates
: |
29/04/2008 |
| Title
: |
GCP Update: Review
of the latest requirements in Europe and US |
|
Reference: |
To ensure clinical trials meet the
requirements of the regulatory authorities it is essential that
trials are carried out to the latest GCP regulatory requirements. It
is particularly important to keep up to date and be familiar with
the recent developments in GCP, and also how these are likely to
impact on trials in the future for both pharmaceutical companies and
the study sites. Regulatory inspectors expect those involved in
clinical trials to be updated with recent developments in GCP ? this
workshop will be ideal for this. This very informative workshop will
take you through the most important recent developments which are
having an impact on clinical trials. Topics include an update on the
latest CT Directive guidelines and other EU GCP developments, and
recent initiatives in the US which are having an impact in Europe.
There will be plenty of time for group discussion of your issues so
as to help you develop you strategies for managing these changes.
|
|
Location : |
London (UK) |
|
Contact : |
Judith Black / Leigh White |
| E-mail : |
info@management-forum.co.uk |
| Phone
: |
+44-1483 730 071 |
| Fax :
|
+44-1483 730 008 |
| More
info : |
www.management-forum.co.uk/html/con_semin_section/con_display_event.asp?event=711 |
| |
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|
