Global Orientation in Conducting Clinical Trials

Wednesday May 28, Thursday May 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 Speakers

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

Valdo Arnera, M.D.
General Manager Europe
PHT Corporation, Switzerland
Web site: www.phtcorp.com

Monica Tocchi, M.D., PH.D.
Executive Medical Director
Meditrial SRL, Italy
Web site: www.meditrialeurope.com

Conference Topics

Wednesday May 28, 2008

Early phases: Phase I and Safety – Part 1
e-clinical trials: Technologies and regulations
Clinical trials: The bridge from fiction to reality

Thursday May 29, 2008

Early phases: Phase I and Safety – Part 2
Pharmacogenetics
Informed consent

Timetable

May 28, 2008 09:00-17:00
May 29, 2008 09:00-16:00

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 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

Contact us

For further information, please contact us at:
Tali Azulay
BioForum CDmC
Phone:     +(972)-8-931-3070
FAX:         +(972)-8-931-3071
E-mail:     talia@bioforumcdmc.com Web site: www.bioforumcdmc.com


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