קטגוריה: ניהול נתונים קליניים - Clinical Data Management , כנסים , ניסויים קליניים
Global Orientation in Conducting Clinical Trials Symposia

 

ניהול מקצועי: גב' טלי אזולאי-אמיר
תאריך: 28, 29 מאי 2008
מיקום הקורס:  מלון דן פנורמה תל אביב
שפת הקורס: עברית
משך הפעילות: 2 ימי לימודים מלאים
שעות:  09:00-17:00
נקודות זכות: 0
מק''ט: 08197
 

Global Orientation in
Conducting Clinical Trials Symposia

May 28- 29, 2008
Dan Panorama Hotel, Tel-Aviv, ISRAEL
Satellite conference of ILSI Biomed Israel 2008

Conference Organizers:

Tali Azulay: talia@bioforumcdmc.com
BioForum CDmC: www.bioforumcdmc.com

Yehudith Wexler: yehudith@bioforum.org.il
BioForum Applied Knowledge Center: www.bioforum.org.il

Dr. Kobi Atsmon: qc@tasmc.health.gov.il
Early Phase Research Center Tel Aviv Sourasky Medical Center: http://www.tasmc.org.il/e

Goal

The conduct of clinical trials is becoming increasingly complex and demanding. Strict international regulations and close public scrutiny drive all parties involved in clinical trials - sponsors, investigators, regulators, coordinators – to keep a watchful eye on the evolving changes and expectations in this area.

Israel has been cultivating a very encouraging atmosphere for novel, health-related high-tech, biotech and pharmaceutical R&D projects. It is only natural that clinical research should be part of it. Indeed, Israel possesses all the basically right "ingredients" for becoming one of the leading countries in this area: highly competent investigators in all relevant clinical fields, state of the art equipment and facilities, high study recruitment rate and awareness of the need to comply with the highest international standards of operation.

The goal of this conference is to highlight topics that are of interest to those involved in clinical trials, either directly or indirectly, aiming in particular to the interactions between local and international "consumers" of this service

Invited Speaker

Michael Owings
Vice President, Quality and Regulatory Compliance
Phase Forward, USA
Web site: www.phaseforward.com

Conference Topics

Wednesday May 28, 2008

  • The changing regulatory environment
  • e-clinical trials: technologies and regulations
  • Statistical trends in clinical research

Thursday May 29, 2008

  • Phase I studies in Israel and in the world
  • Trends in the development of genetic treatments
  • The different aspects of the informed consent procedure

Note: Conference topics are subjected to changes

The agenda will be posted on this site as soon as it is available.

Timetable

May 28, 2008                       09:00-17:00
May 29, 2008                       09:00-17:00

Who Should Attend

Professionals from pharmaceutical, biotech and CROs:

  • Clinical project personnel and leaders
  • Clinical Trials Managers
  • Heads of Clinical Research
  • Clinical Research Associates
  • Clinical/Site Monitors
  • Investigators
  • Clinical trial program and therapeutic area managers
  • QA personnel and managers
  • Regulatory Affairs personnel and managers
  • Clinical Operations personnel and managers
  • Clinical data personnel and managers
  • Clinical statisticians
  • Clinical IT Managers
  • Clinical/Medical Advisors

Registration

Participants are required to register to the ILSI Biomed 2008 conference.
You can register for a single day of for 3 days, as detailed in the web site.
There are significant discounts for students and academics.
The registration fee entitles the participants to attend all other Biomed 2008 events and exhibits.
For more registration details see: http://www.kenes.com/biomed/conference/registration.asp

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